A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13680430



Internal ID21202291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37347145..37347145hg38UCSC Ensembl
chr2:37574288..37574288hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806371
Supporting Variants
Samples
Known GenesQPCT
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13680430
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.6875


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