A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504759



Internal ID20878022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78137768..78138447hg38UCSC Ensembl
chr16:78171665..78172344hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38680
hg19680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032074
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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