A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031688



Internal ID88839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41693521..41701521hg38UCSC Ensembl
chr10:42538688..42546687hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg388001
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143148
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031688
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.714774


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