A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946336



Internal ID31584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23530704..23668205hg38UCSC Ensembl
chr4:23532327..23669828hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38137502
hg19137502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451157
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946336
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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