A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6546n54



Internal ID20139970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54054016..54057172hg38UCSC Ensembl
chr19:54557270..54560426hg19UCSC Ensembl
chr19:59249082..59252238hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383157
hg193157
hg183157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580147, nsv580143, nsv580146, nsv580142, nsv580145
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6546n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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