A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032517



Internal ID19121739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702410..8749652hg38UCSC Ensembl
Innerchr5:8702522..8749764hg19UCSC Ensembl
Innerchr5:8755522..8802764hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3847243
hg1947243
hg1847243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5564n100
Supporting Variantsnssv3746411, nssv3636714, nssv3636730, nssv3636722, nssv3746414, nssv3636713, nssv3746419, nssv3636717, nssv3636729, nssv3746413, nssv3636723, nssv3746418, nssv3636725, nssv3636727, nssv3636735, nssv3636731, nssv3636736, nssv3746409, nssv3746417, nssv3636720, nssv3636712, nssv3636721, nssv3746412, nssv3636728, nssv3636733, nssv3746415, nssv3636737, nssv3636732, nssv3636738, nssv3636724, nssv3636716, nssv3746416, nssv3636726, nssv3746410, nssv3636734, nssv3636715, nssv3636719, nssv3636718
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)nsv1032517
Frequency
Sample Size11257
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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