A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12828n54



Internal ID19005004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104833924..104834705hg38UCSC Ensembl
chr9:107596205..107596986hg19UCSC Ensembl
chr9:106636026..106636807hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38782
hg19782
hg18782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615076, nsv615070, nsv615071
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12828n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer