A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141186



Internal ID19270313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:2041070..2066570hg38UCSC Ensembl
Outerchr11:2062300..2087800hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3825501
hg1925501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959460, nssv3976455
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141186
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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