A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110755



Internal ID21294021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93907093..93909955hg38UCSC Ensembl
Innerchr1:94372649..94375511hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382863
hg192863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085344
Samplessample224
Known GenesGCLM
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110755
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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