A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592702



Internal ID21784745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114266104..114266255hg38UCSC Ensembl
chr10:116025863..116026014hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016180
Supporting Variants
Samples
Known GenesVWA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592702
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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