A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2803529



Internal ID21248867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37677772..37677772hg38UCSC Ensembl
chr21:39050074..39050074hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681344, nssv13681422
Samples
Known GenesKCNJ6
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2803529
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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