A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613745



Internal ID16401154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20404476..20476132hg38UCSC Ensembl
Innerchr9:20404474..20476130hg19UCSC Ensembl
Innerchr9:20394474..20466130hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3871657
hg1971657
hg1871657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1130795
Samples
Known GenesMIR4473, MLLT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613745
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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