A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904379



Internal ID6266306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74884447..75019449hg19UCSC Ensembl
Outerchr15:74869438..75027880hg19UCSC Ensembl
Innerchr15:72671500..72806502hg18UCSC Ensembl
Outerchr15:72656491..72814933hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1543663
SamplesMS16153
Known GenesARID3B, CLK3, CYP1A1, EDC3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904379
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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