A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120085



Internal ID18924664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:47484741..47486161hg38UCSC Ensembl
Outerchr11:47506293..47507713hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381421
hg191421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960832
SamplesKWS1
Known GenesCELF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120085
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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