A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738274



Internal ID161940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3798664..3997055hg38UCSC Ensembl
chrY:3666705..3865096hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38198392
hg19198392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738274
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00125313


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