A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118489



Internal ID18936131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1859870..1864070hg38UCSC Ensembl
Outerchr11:1881100..1885300hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384201
hg194201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958998
SamplesKWS1
Known GenesLSP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118489
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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