A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150360



Internal ID19198084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:122799..145100hg38UCSC Ensembl
Outerchr11:122799..145100hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3822302
hg1922302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003660
SamplesKWB1
Known GenesLINC01001
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150360
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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