A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117704



Internal ID21300970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4874641..4934165hg38UCSC Ensembl
Innerchr2:4922231..4981755hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3859525
hg1959525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102313
Samplessample23
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117704
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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