A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024543



Internal ID84096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79832553..79838806hg38UCSC Ensembl
chr9:82447468..82453721hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg386254
hg196254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024543
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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