A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029694



Internal ID21939037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65581273..65581441hg38UCSC Ensembl
chr15:65873611..65873779hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617232
Samples
Known GenesVWA9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029694
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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