A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951056



Internal ID16953243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:90064933..90097432hg38UCSC Ensembl
Outerchr11:89798101..89830600hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3832500
hg1932500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999603
SamplesBILGI_BIOE
Known GenesUBTFL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951056
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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