A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128659



Internal ID19251992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:109078373..109084473hg38UCSC Ensembl
Outerchr11:108949100..108955200hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg386101
hg196101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960572
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128659
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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