A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110188



Internal ID19278564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:70900..90800hg38UCSC Ensembl
Outerchr11:70900..90800hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3819901
hg1919901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv561n106
Supporting Variantsnssv3959455
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110188
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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