A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738276



Internal ID161942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3842388..3853888hg38UCSC Ensembl
chrY:3710429..3721929hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3811501
hg1911501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738276
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.600627


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