A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637062



Internal ID21829109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21089345..21089526hg38UCSC Ensembl
chr20:21069986..21070167hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056596
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637062
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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