A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149839



Internal ID15531373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669207..15719658hg38UCSC Ensembl
Innerchr19:15780017..15830468hg19UCSC Ensembl
Innerchr19:15641017..15691468hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3850452
hg1950452
hg1850452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578725
Supporting Variants
SamplesHGDP01089
Known GenesCYP4F12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149839
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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