A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738320



Internal ID161986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7609388..7629388hg38UCSC Ensembl
chrY:7477429..7497429hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3820001
hg1920001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738320
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00140944


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