A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1900969



Internal ID17781382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92160689..92161981hg38UCSC Ensembl
Innerchr11:91893855..91895147hg19UCSC Ensembl
Innerchr11:91533503..91534795hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381293
hg191293
hg181293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975218
Supporting Variants
SamplesHGDP00665
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)nssv1900969
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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