A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078189



Internal ID19325845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:13016467..13016520hg38UCSC Ensembl
Outerchr11:13038014..13038067hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766791
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078189
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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