A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578481



Internal ID16019204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6970984..7018169hg38UCSC Ensembl
Innerchr19:6970995..7018180hg19UCSC Ensembl
Innerchr19:6921995..6969180hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3847186
hg1947186
hg1847186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6239n54
Supporting Variantsnssv893210
Samples
Known GenesEMR4P, FLJ25758
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578481
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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