A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615085



Internal ID16055808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104849546..104914659hg38UCSC Ensembl
Innerchr9:107611827..107676940hg19UCSC Ensembl
Innerchr9:106651648..106716761hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3865114
hg1965114
hg1865114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12831n54
Supporting Variantsnssv1176107
Samples1780862197_A
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615085
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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