A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12911n54



Internal ID19005087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130486627..130520222hg38UCSC Ensembl
chr9:133362014..133395609hg19UCSC Ensembl
chr9:132351835..132385430hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3833596
hg1933596
hg1833596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615526, nsv615525
SamplesNINDS_70
Known GenesASS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12911n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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