A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647631



Internal ID21839678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36940950..36944859hg38UCSC Ensembl
chr21:38313250..38317159hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg383910
hg193910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054909
Supporting Variants
Samples
Known GenesHLCS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647631
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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