A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060017



Internal ID18802548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27758162hg38UCSC Ensembl
Innerchr19:27747981..28249070hg19UCSC Ensembl
Innerchr19:32439821..32940910hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38501090
hg19501090
hg18501090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3500n100
Supporting Variantsnssv3572038
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)nsv1060017
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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