A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951021



Internal ID16953208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67283730..67292729hg38UCSC Ensembl
Outerchr11:67051201..67060200hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999569
SamplesBILGI_BIOE
Known GenesADRBK1, ANKRD13D
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951021
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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