A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627632



Internal ID21819679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35564426..35564426hg38UCSC Ensembl
chr20:34152343..34152343hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101297
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627632
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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