A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145876



Internal ID19198260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:20932595..20940403hg38UCSC Ensembl
Outerchr18:18512556..18520364hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg387809
hg197809
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997240
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1145876
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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