A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134159



Internal ID15987345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66844380..66880982hg38UCSC Ensembl
Innerchr9:40811859..40848459hg19UCSC Ensembl
Innerchr9:40801859..40838459hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3836603
hg1936601
hg1836601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614326
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1134159
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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