A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016254



Internal ID19105473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109948521..110027011hg38UCSC Ensembl
Innerchr5:109284222..109362712hg19UCSC Ensembl
Innerchr5:109312121..109390611hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3878491
hg1978491
hg1878491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5777n100
Supporting Variantsnssv3647015
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)nsv1016254
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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