A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601931



Internal ID21793978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42348550..42348550hg38UCSC Ensembl
chr15:42640748..42640748hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093879
Supporting Variants
Samples
Known GenesGANC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601931
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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