A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014354



Internal ID19103573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13363041..13483062hg38UCSC Ensembl
Innerchr2:13503166..13623187hg19UCSC Ensembl
Innerchr2:13420617..13540638hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38120022
hg19120022
hg18120022
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3577050
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)nsv1014354
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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