A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6556n54



Internal ID22774451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54229545..54233134hg38UCSC Ensembl
chr19:54733420..54737010hg19UCSC Ensembl
chr19:59425232..59428822hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383590
hg193591
hg183591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580199, nsv580201, nsv580200
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6556n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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