A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578289



Internal ID16019012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1465535..1469469hg38UCSC Ensembl
Innerchr19:1465534..1469468hg19UCSC Ensembl
Innerchr19:1416534..1420468hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383935
hg193935
hg183935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6201n54
Supporting Variantsnssv891800
Samples
Known GenesAPC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578289
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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