A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140489



Internal ID19281556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110584967..110585057hg38UCSC Ensembl
Outerchr11:110455691..110455781hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv722n106
Supporting Variantsnssv3979570
SamplesKWS2
Known GenesARHGAP20
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140489
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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