A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6201n54



Internal ID18998377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1465535..1470585hg38UCSC Ensembl
chr19:1465534..1470584hg19UCSC Ensembl
chr19:1416534..1421584hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385051
hg195051
hg185051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578290, nsv578289, nsv578292
Samples
Known GenesAPC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6201n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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