A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738379



Internal ID162045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11039488..11376988hg38UCSC Ensembl
chrY:13195164..13532664hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg38337501
hg19337501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138067
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738379
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.622222


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