A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032680



Internal ID19121902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50159790..50225746hg38UCSC Ensembl
Innerchr5:49455624..49521580hg19UCSC Ensembl
Innerchr5:49491381..49557337hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3865957
hg1965957
hg1865957
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5661n100
Supporting Variantsnssv3642055, nssv3642050, nssv3642052, nssv3642054, nssv3642051, nssv3642056, nssv3642053
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)nsv1032680
Frequency
Sample Size11257
Observed Gain6
Observed Loss1
Observed Complex0
Frequencyn/a


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