A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966397



Internal ID44919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33119626..33128864hg38UCSC Ensembl
chr5:33119732..33128970hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg389239
hg199239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140456
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966397
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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