A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6280n54



Internal ID18998456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14621589..14622711hg38UCSC Ensembl
chr19:14732401..14733523hg19UCSC Ensembl
chr19:14593401..14594523hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381123
hg191123
hg181123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578669, nsv578668, nsv578670, nsv578671
Samples
Known GenesEMR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6280n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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