A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021093



Internal ID81700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8164771..8166394hg38UCSC Ensembl
chr9:8164771..8166394hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381624
hg191624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487175
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021093
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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