A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1900285



Internal ID17846414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89552794..89608165hg38UCSC Ensembl
Innerchr11:89285962..89341333hg19UCSC Ensembl
Innerchr11:88925610..88980981hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3855372
hg1955372
hg1855372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv975963
Supporting Variants
SamplesHGDP01029
Known GenesNOX4
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)nssv1900285
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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