A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497836



Internal ID20871044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79159235..79163890hg38UCSC Ensembl
chr16:79193132..79197787hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg384656
hg194656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181730
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497836
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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