A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705607



Internal ID129273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101812066..101970066hg38UCSC Ensembl
chr15:102352269..102510269hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38158001
hg19158001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145681
Supporting Variants
Samples
Known GenesFAM138E, OR4F13P, OR4F15, OR4F4, WASH3P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705607
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001595


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