A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951279



Internal ID16953466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1337871..1491070hg38UCSC Ensembl
Outerchr11:1359101..1512300hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38153200
hg19153200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998121
SamplesBILGI_BIOE
Known GenesBRSK2, MOB2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951279
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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