A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578290



Internal ID16019013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1465535..1470397hg38UCSC Ensembl
Innerchr19:1465534..1470396hg19UCSC Ensembl
Innerchr19:1416534..1421396hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384863
hg194863
hg184863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6201n54
Supporting Variantsnssv891801
Samples
Known GenesAPC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578290
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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