A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615074



Internal ID16055797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104833924..104835365hg38UCSC Ensembl
Innerchr9:107596205..107597646hg19UCSC Ensembl
Innerchr9:106636026..106637467hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381442
hg191442
hg181442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140864
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615074
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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