A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065405



Internal ID19154624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27545499hg38UCSC Ensembl
Innerchr19:27747981..28036407hg19UCSC Ensembl
Innerchr19:32439821..32728247hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38288427
hg19288427
hg18288427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3497n100
Supporting Variantsnssv3571979, nssv3571981, nssv3571980, nssv3571984, nssv3571987, nssv3571982, nssv3571983, nssv3571986, nssv3571988, nssv3571985
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)nsv1065405
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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