A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv896971



Internal ID6303982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6622714..6634659hg19UCSC Ensembl
Outerchr11:6622218..6637235hg19UCSC Ensembl
Innerchr11:6579290..6591235hg18UCSC Ensembl
Outerchr11:6578794..6593811hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510001
SamplesSP54956
Known GenesILK, RRP8, TAF10, TPP1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv896971
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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