A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6289n54



Internal ID20139713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15663105..15724712hg38UCSC Ensembl
chr19:15773915..15835522hg19UCSC Ensembl
chr19:15634915..15696522hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3861608
hg1961608
hg1861608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578727, nsv578724, nsv578725, nsv578728, nsv578720, nsv578726, nsv578719, nsv578729
SamplesHGDP00470, HGDP01413, HGDP00479, HGDP00942, HGDP01414, HGDP01088, HGDP01089, HGDP00459, HGDP00450, HGDP00467, HGDP00466, HGDP00936, HGDP00924, HGDP00940
Known GenesCYP4F12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6289n54
Frequency
Sample Size17421
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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