esv2763822
- Organism: Homo sapiens
- Study:estd203 (Vogler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:40
- Validation:Not tested
- Clinical Assertions: No
- Region Size:9,954
- 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: 530 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 530 SVs from 79 studies. See in: genome view
Overlapping variant regions from other studies: 192 SVs from 26 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 |
---|---|---|---|---|---|---|---|---|---|
esv2763822 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 10,389,091 | 10,399,044 |
esv2763822 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000004.11 | Chr4 | 10,390,715 | 10,400,668 |
esv2763822 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000004.10 | Chr4 | 9,999,813 | 10,009,766 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
---|---|---|---|---|---|
essv7028958 | copy number loss | SW_1079 | SNP array | SNP genotyping analysis | 38 |
essv7028959 | copy number loss | SW_0047 | SNP array | SNP genotyping analysis | 42 |
essv7028960 | copy number loss | SW_0049 | SNP array | SNP genotyping analysis | 49 |
essv7028961 | copy number loss | SW_0063 | SNP array | SNP genotyping analysis | 48 |
essv7028962 | copy number loss | SW_0170 | SNP array | SNP genotyping analysis | 59 |
essv7028963 | copy number loss | SW_0183 | SNP array | SNP genotyping analysis | 45 |
essv7028964 | copy number loss | SW_0184 | SNP array | SNP genotyping analysis | 21 |
essv7028965 | copy number loss | SW_0576 | SNP array | SNP genotyping analysis | 39 |
essv7028966 | copy number loss | SW_0625 | SNP array | SNP genotyping analysis | 41 |
essv7028970 | copy number loss | SW_0632 | SNP array | SNP genotyping analysis | 50 |
essv7028971 | copy number loss | SW_0639 | SNP array | SNP genotyping analysis | 58 |
essv7028972 | copy number loss | SW_0836 | SNP array | SNP genotyping analysis | 50 |
essv7028973 | copy number loss | SW_0871 | SNP array | SNP genotyping analysis | 29 |
essv7028974 | copy number loss | SW_0885 | SNP array | SNP genotyping analysis | 50 |
essv7028975 | copy number loss | SW_1030 | SNP array | SNP genotyping analysis | 27 |
essv7028976 | copy number loss | SW_1085 | SNP array | SNP genotyping analysis | 37 |
essv7028977 | copy number loss | SW_1122 | SNP array | SNP genotyping analysis | 29 |
essv7028978 | copy number loss | SW_1130 | SNP array | SNP genotyping analysis | 33 |
essv7028979 | copy number loss | SW_1134 | SNP array | SNP genotyping analysis | 34 |
essv7028981 | copy number loss | SW_1141 | SNP array | SNP genotyping analysis | 17 |
essv7028982 | copy number loss | SW_1152 | SNP array | SNP genotyping analysis | 19 |
essv7028983 | copy number loss | SW_1203 | SNP array | SNP genotyping analysis | 30 |
essv7028984 | copy number loss | SW_1214 | SNP array | SNP genotyping analysis | 22 |
essv7028985 | copy number loss | SW_1222 | SNP array | SNP genotyping analysis | 29 |
essv7028986 | copy number loss | SW_1224 | SNP array | SNP genotyping analysis | 19 |
essv7028987 | copy number loss | SW_1273 | SNP array | SNP genotyping analysis | 58 |
essv7028988 | copy number loss | SW_1278 | SNP array | SNP genotyping analysis | 28 |
essv7028989 | copy number loss | SW_1341 | SNP array | SNP genotyping analysis | 22 |
essv7028990 | copy number loss | SW_1353 | SNP array | SNP genotyping analysis | 15 |
essv7028992 | copy number loss | SW_1356 | SNP array | SNP genotyping analysis | 26 |
essv7028993 | copy number loss | SW_1361 | SNP array | SNP genotyping analysis | 37 |
essv7028994 | copy number loss | SW_1386 | SNP array | SNP genotyping analysis | 19 |
essv7028995 | copy number loss | SW_1437 | SNP array | SNP genotyping analysis | 29 |
essv7028996 | copy number loss | SW_1464 | SNP array | SNP genotyping analysis | 32 |
essv7028997 | copy number loss | SW_1505 | SNP array | SNP genotyping analysis | 24 |
essv7028998 | copy number loss | SW_1509 | SNP array | SNP genotyping analysis | 36 |
essv7028999 | copy number loss | SW_1523 | SNP array | SNP genotyping analysis | 43 |
essv7029000 | copy number loss | SW_0703 | SNP array | SNP genotyping analysis | 42 |
essv7029001 | copy number loss | SW_1068 | SNP array | SNP genotyping analysis | 44 |
essv7029003 | copy number loss | SW_1387 | SNP array | SNP genotyping analysis | 24 |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv7028958 | Remapped | Perfect | NC_000004.12:g.(?_ 10389091)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,389,091 | 10,399,044 |
essv7028959 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028960 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028961 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028962 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028963 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028964 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028965 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028966 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028970 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028971 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028972 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028973 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028974 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028975 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028976 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028977 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028978 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028979 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028981 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028982 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028983 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028984 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028985 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028986 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028987 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028988 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028989 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028990 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028992 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028993 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028994 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028995 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028996 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028997 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028998 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7028999 | Remapped | Perfect | NC_000004.12:g.(?_ 10390730)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,390,730 | 10,399,044 |
essv7029000 | Remapped | Perfect | NC_000004.12:g.(?_ 10391530)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,391,530 | 10,399,044 |
essv7029001 | Remapped | Perfect | NC_000004.12:g.(?_ 10391530)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,391,530 | 10,399,044 |
essv7029003 | Remapped | Perfect | NC_000004.12:g.(?_ 10391530)_(1039904 4_?)del | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 10,391,530 | 10,399,044 |
essv7028958 | Remapped | Perfect | NC_000004.11:g.(?_ 10390715)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,390,715 | 10,400,668 |
essv7028959 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028960 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028961 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028962 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028963 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028964 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028965 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028966 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028970 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028971 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028972 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028973 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028974 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028975 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028976 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028977 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028978 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028979 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028981 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028982 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028983 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028984 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028985 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028986 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028987 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028988 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028989 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028990 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028992 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028993 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028994 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028995 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028996 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028997 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028998 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7028999 | Remapped | Perfect | NC_000004.11:g.(?_ 10392354)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,392,354 | 10,400,668 |
essv7029000 | Remapped | Perfect | NC_000004.11:g.(?_ 10393154)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,393,154 | 10,400,668 |
essv7029001 | Remapped | Perfect | NC_000004.11:g.(?_ 10393154)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,393,154 | 10,400,668 |
essv7029003 | Remapped | Perfect | NC_000004.11:g.(?_ 10393154)_(1040066 8_?)del | GRCh37.p13 | First Pass | NC_000004.11 | Chr4 | 10,393,154 | 10,400,668 |
essv7028958 | Submitted genomic | NC_000004.10:g.(?_ 9999813)_(10009766 _?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 9,999,813 | 10,009,766 | ||
essv7028959 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028960 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028961 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028962 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028963 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028964 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028965 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028966 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028970 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028971 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028972 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028973 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028974 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028975 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028976 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028977 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028978 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028979 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 | ||
essv7028981 | Submitted genomic | NC_000004.10:g.(?_ 10001452)_(1000976 6_?)del | NCBI36 (hg18) | NC_000004.10 | Chr4 | 10,001,452 | 10,009,766 |