A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504976



Internal ID20878241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101786563..101920085hg38UCSC Ensembl
chr15:102326766..102460288hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38133523
hg19133523
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184497
Samples
Known GenesOR4F13P, OR4F15, OR4F6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504976
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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