A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742986



Internal ID166652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:24881334..24896057hg38UCSC Ensembl
chrY:27027481..27042204hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3814724
hg1914724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138081
Supporting Variants
Samples
Known GenesDAZ2, DAZ3, DAZ4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742986
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00820793


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