A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020163



Internal ID81076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26947364..26947560hg38UCSC Ensembl
chr9:26947362..26947558hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489369
Supporting Variants
Samples
Known GenesIFT74, PLAA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020163
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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