A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615089



Internal ID16055812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104858106..104863908hg38UCSC Ensembl
Innerchr9:107620387..107626189hg19UCSC Ensembl
Innerchr9:106660208..106666010hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385803
hg195803
hg185803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140900
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615089
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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