A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111158



Internal ID19285832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:59705526..59708842hg38UCSC Ensembl
Outerchr18:57372758..57376074hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg383317
hg193317
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962402
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111158
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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