A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496108



Internal ID20869306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78203802..78389557hg38UCSC Ensembl
chr16:78237699..78423454hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38185756
hg19185756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032078
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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