A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626603



Internal ID21818650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34937510..34937510hg38UCSC Ensembl
chr20:33525313..33525313hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102976
Supporting Variants
Samples
Known GenesGSS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626603
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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