A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6462n54



Internal ID20139886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42752863..42889774hg38UCSC Ensembl
chr19:43257015..43393926hg19UCSC Ensembl
chr19:47948855..48085766hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38136912
hg19136912
hg18136912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579636, nsv579648
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6462n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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