A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613220



Internal ID21805267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41109190..41111180hg38UCSC Ensembl
chr15:41401388..41403378hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381991
hg191991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029315
Supporting Variants
Samples
Known GenesINO80
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613220
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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