A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496379



Internal ID20869580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78144082..78314242hg38UCSC Ensembl
chr16:78177979..78348139hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38170161
hg19170161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193599
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496379
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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