A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037612



Internal ID92828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97437504..97437612hg38UCSC Ensembl
chr10:99197261..99197369hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478096
Supporting Variants
Samples
Known GenesEXOSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037612
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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