A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140892



Internal ID15647392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104842441..104871444hg38UCSC Ensembl
Innerchr9:107604722..107633725hg19UCSC Ensembl
Innerchr9:106644543..106673546hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3829004
hg1929004
hg1829004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615083
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)nssv1140892
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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