A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578725



Internal ID16019448
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 StatusM
Merged Variantsdgv6289n54
Supporting Variantsnssv1149839, nssv1149840, nssv1149838
SamplesHGDP01414, HGDP01089, HGDP00924
Known GenesCYP4F12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578725
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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