A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028449



Internal ID19117667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109932371..110017900hg38UCSC Ensembl
Innerchr5:109268072..109353601hg19UCSC Ensembl
Innerchr5:109295971..109381500hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3885530
hg1985530
hg1885530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5777n100
Supporting Variantsnssv3647010
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)nsv1028449
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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