A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6537n54



Internal ID20139961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53419262..53519471hg38UCSC Ensembl
chr19:53922515..54022725hg19UCSC Ensembl
chr19:58614327..58714537hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38100210
hg19100211
hg18100211
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580100, nsv580087, nsv580096, nsv580090, nsv580098, nsv580089, nsv580088, nsv580099, nsv580103, nsv580091, nsv580094
SamplesHGDP00699, 1780854540_A, HGDP00783, 1780854480_A
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6537n54
Frequency
Sample Size17421
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer