A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178852



Internal ID20745892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101676704..101819711hg38UCSC Ensembl
chr15:102216907..102359914hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38143008
hg19143008
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502330
Supporting Variants
Samples
Known GenesOR4F15, OR4F6, TARSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178852
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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