A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699292



Internal ID21221140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134329151..134329151hg38UCSC Ensembl
chr3:134047993..134047993hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699292
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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