A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684034



Internal ID21205889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31199765..31199765hg38UCSC Ensembl
chr19:31690671..31690671hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2799599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684034
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.596774


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