A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12568n54



Internal ID20145992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12628213..12712157hg38UCSC Ensembl
chr9:12628213..12712157hg19UCSC Ensembl
chr9:12618213..12702157hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3883945
hg1983945
hg1883945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613611, nsv613612
Samples
Known GenesTYRP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12568n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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