A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125339



Internal ID19260563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:65306574..65306739hg38UCSC Ensembl
Outerchr11:65074045..65074210hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983515
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125339
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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