A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033972



Internal ID19123194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10833580..10964559hg38UCSC Ensembl
Innerchr5:10833692..10964671hg19UCSC Ensembl
Innerchr5:10886692..11017671hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38130980
hg19130980
hg18130980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5569n100
Supporting Variantsnssv3638199
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)nsv1033972
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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