A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496466



Internal ID20869668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36554734..36585271hg38UCSC Ensembl
chr15:36846935..36877472hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3830538
hg1930538
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191605
Samples
Known GenesC15orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496466
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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