A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010726



Internal ID74779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40496743..40496800hg38UCSC Ensembl
chr8:40354262..40354319hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010726
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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