A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505929



Internal ID20879203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79041302..79073680hg38UCSC Ensembl
chr16:79075199..79107577hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3832379
hg1932379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032182
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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