A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111822



Internal ID21295088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87218642..87905196hg38UCSC Ensembl
Innerchr2:87445765..88204715hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38686555
hg19758951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102510
Samplessample60
Known GenesLINC00152, MIR4435-1, MIR4435-2, PLGLB1, PLGLB2, RGPD1, RGPD2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111822
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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