A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700162



Internal ID123828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41109224..41111300hg38UCSC Ensembl
chr15:41401422..41403498hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382077
hg192077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146204
Supporting Variants
Samples
Known GenesINO80
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700162
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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