A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698177



Internal ID21220031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43076801..43076801hg38UCSC Ensembl
chr15:43368999..43368999hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795240
Supporting Variants
Samples
Known GenesUBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698177
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.741935


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