A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697194



Internal ID21219044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38930731..38930731hg38UCSC Ensembl
chr17:37086984..37086984hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797464
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697194
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.887097


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