A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014859



Internal ID18757394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:115439375..116181008hg38UCSC Ensembl
Innerchr2:116196951..116938584hg19UCSC Ensembl
Innerchr2:115913421..116655054hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38741634
hg19741634
hg18741634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3580268
Samples
Known GenesDPP10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014859
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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