A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615087



Internal ID16055810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104856400..104886371hg38UCSC Ensembl
Innerchr9:107618681..107648652hg19UCSC Ensembl
Innerchr9:106658502..106688473hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3829972
hg1929972
hg1829972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12832n54
Supporting Variantsnssv1140898, nssv1140897
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615087
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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