A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631682



Internal ID21823729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38649562..38649562hg38UCSC Ensembl
chr20:37278205..37278205hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103547
Supporting Variants
Samples
Known GenesARHGAP40
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631682
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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