A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615086



Internal ID16055809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104856400..104864978hg38UCSC Ensembl
Innerchr9:107618681..107627259hg19UCSC Ensembl
Innerchr9:106658502..106667080hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg388579
hg198579
hg188579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140896
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615086
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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