A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034790



Internal ID19124011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:34258374..34484048hg38UCSC Ensembl
Innerchr5:34258479..34484153hg19UCSC Ensembl
Innerchr5:34294236..34519910hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38225675
hg19225675
hg18225675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5628n100
Supporting Variantsnssv3637062
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)nsv1034790
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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