A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv897314



Internal ID6304325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45827350..45939641hg19UCSC Ensembl
Outerchr11:45816020..45965129hg19UCSC Ensembl
Innerchr11:45783926..45896217hg18UCSC Ensembl
Outerchr11:45772596..45921705hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1530721
SamplesMS10311
Known GenesC11orf94, CRY2, GYLTL1B, MAPK8IP1, PEX16, PHF21A, SLC35C1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv897314
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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