A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13695665



Internal ID21217516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62954367..62954367hg38UCSC Ensembl
chr3:62940042..62940042hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809484
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13695665
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.015625


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer