A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059313



Internal ID19148532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27582039hg38UCSC Ensembl
Innerchr19:27747981..28072947hg19UCSC Ensembl
Innerchr19:32439821..32764787hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38324967
hg19324967
hg18324967
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3497n100
Supporting Variantsnssv3572019, nssv3572017, nssv3572018
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)nsv1059313
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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