A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904380



Internal ID6266307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74884447..75133220hg19UCSC Ensembl
Outerchr15:74869438..75142761hg19UCSC Ensembl
Innerchr15:72671500..72920273hg18UCSC Ensembl
Outerchr15:72656491..72929814hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1546873, nssv1530812
SamplesMS10311, MS17208
Known GenesARID3B, CLK3, CPLX3, CSK, CYP1A1, CYP1A2, EDC3, LMAN1L, MIR4513, SCAMP2, ULK3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904380
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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