A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503931



Internal ID20877189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36447467..36782964hg38UCSC Ensembl
chr15:36739668..37075165hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38335498
hg19335498
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180559
Samples
Known GenesC15orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503931
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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