A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141189



Internal ID19277492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:10173653..10179753hg38UCSC Ensembl
Outerchr11:10195200..10201300hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386101
hg196101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992695
SamplesKWS2
Known GenesSBF2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141189
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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