A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001966



Internal ID19091183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87249441..87661069hg38UCSC Ensembl
Innerchr2:87476564..87960588hg19UCSC Ensembl
Innerchr2:87330075..87741703hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38411629
hg19484025
hg18411629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3900n100
Supporting Variantsnssv3728776
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001966
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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