A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510243



Internal ID20883560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79190401..79238100hg38UCSC Ensembl
chr16:79224298..79271997hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3847700
hg1947700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2945n223
Supporting Variantsnssv18032191
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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