A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703449



Internal ID127115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101616066..101969066hg38UCSC Ensembl
chr15:102156269..102509269hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38353001
hg19353001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521354
Supporting Variants
Samples
Known GenesFAM138E, OR4F13P, OR4F15, OR4F4, OR4F6, TARSL2, TM2D3, WASH3P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703449
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000469


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