A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13680140



Internal ID21202004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40374557..40374557hg38UCSC Ensembl
chr15:40666758..40666758hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13680140
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.125


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