A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738267



Internal ID161933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2781388..3953388hg38UCSC Ensembl
chrY:2649429..3821429hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg381172001
hg191172001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431133
Supporting Variants
Samples
Known GenesLINC00278, RPS4Y1, SRY, TGIF2LY, ZFY
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738267
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00188679


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