A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009638



Internal ID74070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39897753..39905085hg38UCSC Ensembl
chr8:39755272..39762604hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg387333
hg197333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492282
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009638
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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