A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13701674



Internal ID21223500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39894053..39894053hg38UCSC Ensembl
chr15:40186254..40186254hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795065
Supporting Variants
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13701674
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.983871


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