A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13680250



Internal ID21202092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156660553..156660553hg38UCSC Ensembl
chr4:157581705..157581705hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13680250
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.53125


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