esv2763254
- Organism: Homo sapiens
- Study:estd203 (Vogler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:37
- Validation:Not tested
- Clinical Assertions: No
- Region Size:13,368
- Publication(s):Vogler et al. 2010
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 345 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 345 SVs from 59 studies. See in: genome view
Overlapping variant regions from other studies: 145 SVs from 20 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2763254 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000002.12 | Chr2 | 183,219,425 | 183,232,792 |
| esv2763254 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000002.11 | Chr2 | 184,084,153 | 184,097,520 |
| esv2763254 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000002.10 | Chr2 | 183,792,398 | 183,805,765 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv7020978 | copy number loss | SW_0113 | SNP array | SNP genotyping analysis | 47 |
| essv7020989 | copy number loss | SW_0149 | SNP array | SNP genotyping analysis | 38 |
| essv7021000 | copy number loss | SW_1269 | SNP array | SNP genotyping analysis | 17 |
| essv7021011 | copy number loss | SW_1294 | SNP array | SNP genotyping analysis | 32 |
| essv7021022 | copy number loss | SW_0007 | SNP array | SNP genotyping analysis | 53 |
| essv7021033 | copy number loss | SW_0032 | SNP array | SNP genotyping analysis | 58 |
| essv7021044 | copy number loss | SW_0043 | SNP array | SNP genotyping analysis | 35 |
| essv7021055 | copy number loss | SW_0187 | SNP array | SNP genotyping analysis | 30 |
| essv7021066 | copy number loss | SW_0203 | SNP array | SNP genotyping analysis | 49 |
| essv7021078 | copy number loss | SW_0270 | SNP array | SNP genotyping analysis | 25 |
| essv7021089 | copy number loss | SW_0352 | SNP array | SNP genotyping analysis | 35 |
| essv7021100 | copy number loss | SW_0570 | SNP array | SNP genotyping analysis | 39 |
| essv7021111 | copy number loss | SW_0790 | SNP array | SNP genotyping analysis | 48 |
| essv7021122 | copy number loss | SW_0791 | SNP array | SNP genotyping analysis | 38 |
| essv7021133 | copy number loss | SW_0805 | SNP array | SNP genotyping analysis | 42 |
| essv7021144 | copy number loss | SW_0820 | SNP array | SNP genotyping analysis | 34 |
| essv7021155 | copy number loss | SW_1000 | SNP array | SNP genotyping analysis | 42 |
| essv7021166 | copy number loss | SW_1003 | SNP array | SNP genotyping analysis | 34 |
| essv7021177 | copy number loss | SW_1006 | SNP array | SNP genotyping analysis | 34 |
| essv7021189 | copy number loss | SW_1013 | SNP array | SNP genotyping analysis | 32 |
| essv7021200 | copy number loss | SW_1063 | SNP array | SNP genotyping analysis | 50 |
| essv7021211 | copy number loss | SW_1070 | SNP array | SNP genotyping analysis | 37 |
| essv7021222 | copy number loss | SW_1088 | SNP array | SNP genotyping analysis | 37 |
| essv7021233 | copy number loss | SW_1127 | SNP array | SNP genotyping analysis | 34 |
| essv7021244 | copy number loss | SW_1153 | SNP array | SNP genotyping analysis | 48 |
| essv7021255 | copy number loss | SW_1188 | SNP array | SNP genotyping analysis | 32 |
| essv7021266 | copy number loss | SW_1192 | SNP array | SNP genotyping analysis | 29 |
| essv7021277 | copy number loss | SW_1266 | SNP array | SNP genotyping analysis | 20 |
| essv7021288 | copy number loss | SW_1325 | SNP array | SNP genotyping analysis | 28 |
| essv7021300 | copy number loss | SW_1348 | SNP array | SNP genotyping analysis | 26 |
| essv7021311 | copy number loss | SW_1355 | SNP array | SNP genotyping analysis | 37 |
| essv7021322 | copy number loss | SW_1455 | SNP array | SNP genotyping analysis | 39 |
| essv7021333 | copy number loss | SW_1476 | SNP array | SNP genotyping analysis | 44 |
| essv7021344 | copy number loss | SW_1511 | SNP array | SNP genotyping analysis | 31 |
| essv7021355 | copy number loss | SW_1060 | SNP array | SNP genotyping analysis | 34 |
| essv7021366 | copy number loss | SW_0145 | SNP array | SNP genotyping analysis | 56 |
| essv7021377 | copy number loss | SW_1282 | SNP array | SNP genotyping analysis | 48 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv7020978 | Remapped | Perfect | NC_000002.12:g.(?_ 183219425)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,219,425 | 183,224,996 |
| essv7020989 | Remapped | Perfect | NC_000002.12:g.(?_ 183219425)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,219,425 | 183,224,996 |
| essv7021000 | Remapped | Perfect | NC_000002.12:g.(?_ 183219425)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,219,425 | 183,224,996 |
| essv7021011 | Remapped | Perfect | NC_000002.12:g.(?_ 183219425)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,219,425 | 183,224,996 |
| essv7021022 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021033 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021044 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021055 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021066 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021078 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021089 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021100 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021111 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021122 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021133 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021144 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021155 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021166 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021177 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021189 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021200 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021211 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021222 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021233 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021244 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021255 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021266 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021277 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021288 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021300 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021311 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021322 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021333 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021344 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,224,996 |
| essv7021355 | Remapped | Perfect | NC_000002.12:g.(?_ 183220725)_(183232 792_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,220,725 | 183,232,792 |
| essv7021366 | Remapped | Perfect | NC_000002.12:g.(?_ 183221060)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,221,060 | 183,224,996 |
| essv7021377 | Remapped | Perfect | NC_000002.12:g.(?_ 183221060)_(183224 996_?)del | GRCh38.p12 | First Pass | NC_000002.12 | Chr2 | 183,221,060 | 183,224,996 |
| essv7020978 | Remapped | Perfect | NC_000002.11:g.(?_ 184084153)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,084,153 | 184,089,724 |
| essv7020989 | Remapped | Perfect | NC_000002.11:g.(?_ 184084153)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,084,153 | 184,089,724 |
| essv7021000 | Remapped | Perfect | NC_000002.11:g.(?_ 184084153)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,084,153 | 184,089,724 |
| essv7021011 | Remapped | Perfect | NC_000002.11:g.(?_ 184084153)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,084,153 | 184,089,724 |
| essv7021022 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021033 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021044 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021055 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021066 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021078 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021089 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021100 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021111 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021122 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021133 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021144 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021155 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021166 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021177 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021189 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021200 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021211 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021222 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021233 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021244 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021255 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021266 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021277 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021288 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021300 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021311 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021322 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021333 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021344 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,089,724 |
| essv7021355 | Remapped | Perfect | NC_000002.11:g.(?_ 184085453)_(184097 520_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,453 | 184,097,520 |
| essv7021366 | Remapped | Perfect | NC_000002.11:g.(?_ 184085788)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,788 | 184,089,724 |
| essv7021377 | Remapped | Perfect | NC_000002.11:g.(?_ 184085788)_(184089 724_?)del | GRCh37.p13 | First Pass | NC_000002.11 | Chr2 | 184,085,788 | 184,089,724 |
| essv7020978 | Submitted genomic | NC_000002.10:g.(?_ 183792398)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,792,398 | 183,797,969 | ||
| essv7020989 | Submitted genomic | NC_000002.10:g.(?_ 183792398)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,792,398 | 183,797,969 | ||
| essv7021000 | Submitted genomic | NC_000002.10:g.(?_ 183792398)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,792,398 | 183,797,969 | ||
| essv7021011 | Submitted genomic | NC_000002.10:g.(?_ 183792398)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,792,398 | 183,797,969 | ||
| essv7021022 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021033 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021044 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021055 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021066 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021078 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021089 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021100 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021111 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021122 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021133 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021144 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021155 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021166 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021177 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021189 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021200 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021211 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021222 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021233 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021244 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 | ||
| essv7021255 | Submitted genomic | NC_000002.10:g.(?_ 183793698)_(183797 969_?)del | NCBI36 (hg18) | NC_000002.10 | Chr2 | 183,793,698 | 183,797,969 |