A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682960



Internal ID21204818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60255309..60255309hg38UCSC Ensembl
chr13:60829443..60829443hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793873
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682960
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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