A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032052



Internal ID89073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15050831..15051163hg38UCSC Ensembl
chr10:15092830..15093162hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473953
Supporting Variants
Samples
Known GenesOLAH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032052
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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