A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611679



Internal ID21803726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63744126..63744180hg38UCSC Ensembl
chr15:64036325..64036379hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035465
Supporting Variants
Samples
Known GenesHERC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611679
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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