A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678073



Internal ID21199928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90819209..90819209hg38UCSC Ensembl
chr15:91362439..91362439hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795402
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678073
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.289474


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