A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931298



Internal ID22706580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78575326..78828202hg38UCSC Ensembl
chr16:78609223..78862099hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38252877
hg19252877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381602
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931298
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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