A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120116



Internal ID18934579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:55478831..55505522hg38UCSC Ensembl
Outerchr18:53146062..53172753hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3826692
hg1926692
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960870
SamplesKWS1
Known GenesMIR4529, TCF4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120116
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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