A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6281n54



Internal ID18998457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14621589..14623149hg38UCSC Ensembl
chr19:14732401..14733961hg19UCSC Ensembl
chr19:14593401..14594961hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381561
hg191561
hg181561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578672, nsv578673, nsv578675, nsv578674, nsv578677, nsv578678
Samples
Known GenesEMR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6281n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss45
Observed Complex0
Frequencyn/a


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