A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033551



Internal ID90057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45676345..45680268hg38UCSC Ensembl
chr10:46171793..46175716hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg383924
hg193924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033551
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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