A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117740



Internal ID21301006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:201200364..201210699hg38UCSC Ensembl
Innerchr2:202065087..202075422hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3810336
hg1910336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105881
Samplessample246
Known GenesCASP10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117740
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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