A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643582



Internal ID21835629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38247062..38247122hg38UCSC Ensembl
chr21:39618984..39619044hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059501
Supporting Variants
Samples
Known GenesKCNJ15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643582
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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