A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904099



Internal ID6266026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40952261..41029667hg19UCSC Ensembl
Outerchr15:40949526..41041875hg19UCSC Ensembl
Innerchr15:38739553..38816959hg18UCSC Ensembl
Outerchr15:38736818..38829167hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1597841
SamplesIS41317
Known GenesCASC5, FAM82A2, LOC100505648, RAD51
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904099
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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