A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681422



Internal ID21203283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37677772..37677772hg38UCSC Ensembl
chr21:39050074..39050074hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803529
Supporting Variants
Samples
Known GenesKCNJ6
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681422
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.96


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