A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13710608



Internal ID21232373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:72017602..72017602hg38UCSC Ensembl
chr2:72244732..72244732hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806999
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13710608
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0862069


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