A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132352



Internal ID18935798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110209375..110214775hg38UCSC Ensembl
Outerchr11:110080100..110085500hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg385401
hg195401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv721n106
Supporting Variantsnssv3987125
SamplesKWS1
Known GenesRDX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132352
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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