A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17016749



Internal ID78821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110029020..110035899hg38UCSC Ensembl
chr8:111041249..111048128hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg386880
hg196880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475266
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17016749
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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