A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117053



Internal ID21300319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92688299..92690922hg38UCSC Ensembl
Innerchr10:94448056..94450679hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg382624
hg192624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088610
Samplessample224
Known GenesHHEX
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117053
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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