nsv5665124
- Organism: Homo sapiens
- Study:nstd207 (Ebert et al. 2021)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:127,232
- Publication(s):Ebert et al. 2021
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: 633 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 633 SVs from 47 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv5665124 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000023.11 | ChrX | 127,625,450 | 127,752,681 | ||
nsv5665124 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000023.10 | ChrX | 126,759,431 | 126,886,662 |
Variant Call Information
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv17165480 | Submitted genomic | NC_000023.11:g.127 625450_127752681de lA | GRCh38 (hg38) | NC_000023.11 | ChrX | 127,625,450 | 127,752,681 | ||
nssv17165480 | Remapped | Perfect | NC_000023.10:g.126 759431_126886662de lA | GRCh37.p13 | First Pass | NC_000023.10 | ChrX | 126,759,431 | 126,886,662 |