A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020838



Internal ID81542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19642692..19642980hg38UCSC Ensembl
chr9:19642690..19642978hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142396
Supporting Variants
Samples
Known GenesSLC24A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020838
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003123


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