A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17685983



Internal ID109649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20881562..20884011hg38UCSC Ensembl
chr13:21455701..21458150hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382450
hg192450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502152
Supporting Variants
Samples
Known GenesXPO4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17685983
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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