A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6456n54



Internal ID20139880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41554997..41555814hg38UCSC Ensembl
chr19:42061367..42062184hg19UCSC Ensembl
chr19:46753207..46754024hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38818
hg19818
hg18818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579613, nsv579612, nsv579610, nsv579611, nsv579614
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6456n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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