A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036594



Internal ID92142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95447028..95448268hg38UCSC Ensembl
chr10:97206785..97208025hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381241
hg191241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476733
Supporting Variants
Samples
Known GenesSORBS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036594
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.678014


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