A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1890310



Internal ID17827285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56511969..56513205hg38UCSC Ensembl
Innerchr11:56279445..56280681hg19UCSC Ensembl
Innerchr11:56036021..56037257hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg381237
hg191237
hg181237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv975928
Supporting Variants
SamplesHGDP00998
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1890310
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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