A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962257



Internal ID42136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184964974..184966849hg38UCSC Ensembl
chr4:185886128..185888003hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381876
hg191876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140488
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962257
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008305


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