A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17006764



Internal ID72128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9886203..9892687hg38UCSC Ensembl
chr8:9743713..9750197hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386485
hg196485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484950
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17006764
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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