A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708705



Internal ID132371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78224015..78356466hg38UCSC Ensembl
chr16:78257912..78390363hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38132452
hg19132452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514872
Supporting Variants
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708705
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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