A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12830n54



Internal ID19005006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104836459..104871444hg38UCSC Ensembl
chr9:107598740..107633725hg19UCSC Ensembl
chr9:106638561..106673546hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3834986
hg1934986
hg1834986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615081, nsv615080, nsv615083
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12830n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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