A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049659



Internal ID21958892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37717429..37717483hg38UCSC Ensembl
chr21:39089732..39089786hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648280
Samples
Known GenesKCNJ6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049659
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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