A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013460



Internal ID19102678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:81969821..82086876hg38UCSC Ensembl
Innerchr2:82196945..82314000hg19UCSC Ensembl
Innerchr2:82050456..82167511hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38117056
hg19117056
hg18117056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3884n100
Supporting Variantsnssv3582135
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013460
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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