A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951302



Internal ID17300176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:5808171..5819770hg38UCSC Ensembl
Outerchr11:5829401..5841000hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811600
hg1911600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998144
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951302
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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