A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17006769



Internal ID72131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9909038..9909089hg38UCSC Ensembl
chr8:9766548..9766599hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488951
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17006769
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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