A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1891132



Internal ID17847108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60078272..60086204hg38UCSC Ensembl
Innerchr11:59845745..59853677hg19UCSC Ensembl
Innerchr11:59602321..59610253hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg387933
hg197933
hg187933
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972036
Supporting Variants
SamplesHGDP01029
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1891132
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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