A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133000



Internal ID18924415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:89827620..90017102hg38UCSC Ensembl
Outerchr11:89560788..89750270hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38189483
hg19189483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987797
SamplesKWS1
Known GenesMIR5692A1, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133000
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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