A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033605



Internal ID19122826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:109932371..110027871hg38UCSC Ensembl
Innerchr5:109268072..109363572hg19UCSC Ensembl
Innerchr5:109295971..109391471hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3895501
hg1995501
hg1895501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5777n100
Supporting Variantsnssv3746558
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)nsv1033605
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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