A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962188



Internal ID42091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183184868..183185148hg38UCSC Ensembl
chr4:184106021..184106301hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467586
Supporting Variants
Samples
Known GenesWWC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962188
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00281


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