A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13692612



Internal ID21214464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128150946..128150946hg38UCSC Ensembl
chr3:127869789..127869789hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13692612
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.21875


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