A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615088



Internal ID16055811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104858051..104893567hg38UCSC Ensembl
Innerchr9:107620332..107655848hg19UCSC Ensembl
Innerchr9:106660153..106695669hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3835517
hg1935517
hg1835517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12832n54
Supporting Variantsnssv1140899
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615088
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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