A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13686482



Internal ID21208338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184713008..184713008hg38UCSC Ensembl
chr3:184430796..184430796hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2808145
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13686482
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.395833


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