A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6239n54



Internal ID20139663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6957866..7018858hg38UCSC Ensembl
chr19:6957877..7018869hg19UCSC Ensembl
chr19:6908877..6969869hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3860993
hg1960993
hg1860993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578475, nsv578479, nsv578481, nsv578480
Samples
Known GenesEMR4P, FLJ25758
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6239n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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