A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582733



Internal ID16370142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:115678798..115938858hg38UCSC Ensembl
Innerchr2:116436374..116696434hg19UCSC Ensembl
Innerchr2:116152844..116412904hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38260061
hg19260061
hg18260061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv916286
Samples
Known GenesDPP10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582733
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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