A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705603



Internal ID129269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101786000..101980066hg38UCSC Ensembl
chr15:102326203..102520269hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38194067
hg19194067
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145109
Supporting Variants
Samples
Known GenesDDX11L9, FAM138E, MIR6859-1, MIR6859-2, OR4F13P, OR4F15, OR4F4, OR4F6, WASH3P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705603
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000938


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