A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578728



Internal ID16019451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15670671..15718554hg38UCSC Ensembl
Innerchr19:15781481..15829364hg19UCSC Ensembl
Innerchr19:15642481..15690364hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3847884
hg1947884
hg1847884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6289n54
Supporting Variantsnssv1149846
SamplesHGDP00479
Known GenesCYP4F12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578728
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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