A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579524



Internal ID16366933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39896716..39906245hg38UCSC Ensembl
Innerchr19:40387356..40396621hg19UCSC Ensembl
Innerchr19:45079196..45088461hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg389530
hg199266
hg189266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899387, nssv899386
Samples
Known GenesFCGBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579524
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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