A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507393



Internal ID20880683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101719001..101868300hg38UCSC Ensembl
chr15:102259204..102408503hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38149300
hg19149300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178394
Samples
Known GenesOR4F13P, OR4F15, OR4F6, TARSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507393
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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