A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140884



Internal ID15647384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104834004..104834815hg38UCSC Ensembl
Innerchr9:107596285..107597096hg19UCSC Ensembl
Innerchr9:106636106..106636917hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38812
hg19812
hg18812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615077
Supporting Variants
Samples
Known GenesABCA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1140884
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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