A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1892709



Internal ID17868364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62010984..62012715hg38UCSC Ensembl
Innerchr11:61778456..61780187hg19UCSC Ensembl
Innerchr11:61535032..61536763hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381732
hg191732
hg181732
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975937
Supporting Variants
SamplesHGDP01284
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)nssv1892709
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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