A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578651



Internal ID16019374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14089297..14091875hg38UCSC Ensembl
Innerchr19:14200109..14202687hg19UCSC Ensembl
Innerchr19:14061109..14063687hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382579
hg192579
hg182579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6276n54
Supporting Variantsnssv894822
Samples
Known GenesPRKACA, SAMD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578651
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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