A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615078



Internal ID16055801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104834004..104834976hg38UCSC Ensembl
Innerchr9:107596285..107597257hg19UCSC Ensembl
Innerchr9:106636106..106637078hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38973
hg19973
hg18973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12829n54
Supporting Variantsnssv1140887
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615078
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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