A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738416



Internal ID162082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12509925..12520385hg38UCSC Ensembl
chrY:14621727..14632316hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3810461
hg1910590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738416
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00125313


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer