A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578724



Internal ID16019447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669207..15718554hg38UCSC Ensembl
Innerchr19:15780017..15829364hg19UCSC Ensembl
Innerchr19:15641017..15690364hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3849348
hg1949348
hg1849348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6289n54
Supporting Variantsnssv1149835, nssv1149836, nssv1149834, nssv895576, nssv1149837, nssv895577
SamplesHGDP00470, HGDP01088, HGDP00936, HGDP00940
Known GenesCYP4F12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578724
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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