A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010531



Internal ID74647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36310962..36316649hg38UCSC Ensembl
chr8:36168480..36174167hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg385688
hg195688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010531
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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