A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133066



Internal ID18930029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29819009..29819076hg38UCSC Ensembl
Outerchr19:30309916..30309983hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987875
SamplesKWS1
Known GenesCCNE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133066
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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