esv3692867
- Organism: Homo sapiens
- Study:estd221 (Palta et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:2
- Validation:Not tested
- Clinical Assertions: No
- Region Size:60,611
- Publication(s):Palta et al. 2015
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: 302 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 302 SVs from 56 studies. See in: genome view
Overlapping variant regions from other studies: 97 SVs from 18 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
esv3692867 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000005.10 | Chr5 | 98,141,523 | 98,202,133 |
esv3692867 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000005.9 | Chr5 | 97,477,227 | 97,537,837 |
esv3692867 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000005.8 | Chr5 | 97,502,983 | 97,563,593 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
---|---|---|---|---|---|---|---|---|---|
essv16507613 | Remapped | Perfect | NC_000005.10:g.(?_ 98141523)_(9820213 3_?)dup | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 98,141,523 | 98,202,133 |
essv16508118 | Remapped | Perfect | NC_000005.10:g.(?_ 98161725)_(9820213 3_?)dup | GRCh38.p12 | First Pass | NC_000005.10 | Chr5 | 98,161,725 | 98,202,133 |
essv16507613 | Remapped | Perfect | NC_000005.9:g.(?_9 7477227)_(97537837 _?)dup | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 97,477,227 | 97,537,837 |
essv16508118 | Remapped | Perfect | NC_000005.9:g.(?_9 7497429)_(97537837 _?)dup | GRCh37.p13 | First Pass | NC_000005.9 | Chr5 | 97,497,429 | 97,537,837 |
essv16507613 | Submitted genomic | NC_000005.8:g.(?_9 7502983)_(97563593 _?)dup | NCBI36 (hg18) | NC_000005.8 | Chr5 | 97,502,983 | 97,563,593 | ||
essv16508118 | Submitted genomic | NC_000005.8:g.(?_9 7523185)_(97563593 _?)dup | NCBI36 (hg18) | NC_000005.8 | Chr5 | 97,523,185 | 97,563,593 |