A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495937



Internal ID20869133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36532058..36566850hg38UCSC Ensembl
chr15:36824259..36859051hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3834793
hg1934793
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495937
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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