A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020792



Internal ID81506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18942027..18942109hg38UCSC Ensembl
chr9:18942025..18942107hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479810
Supporting Variants
Samples
Known GenesFAM154A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020792
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.146939


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