A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111677



Internal ID21294943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44273233..44299970hg38UCSC Ensembl
Innerchr2:44500372..44527109hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3826738
hg1926738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105161
Samplessample262
Known GenesSLC3A1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111677
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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