A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115633



Internal ID21298899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:109243050..109319672hg38UCSC Ensembl
Innerchr2:109859506..109936128hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg3876623
hg1976623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104634
Samplessample141
Known GenesMIR4266, SH3RF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115633
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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