A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035673



Internal ID91527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76619070..76621106hg38UCSC Ensembl
chr10:78378828..78380864hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382037
hg192037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035673
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002498


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