A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17006770



Internal ID72132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9933932..9946126hg38UCSC Ensembl
chr8:9791442..9803636hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3812195
hg1912195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17006770
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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