A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612865



Internal ID21804912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26417396..26417396hg38UCSC Ensembl
chr15:26662543..26662543hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095755
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612865
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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