A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1874476



Internal ID17779684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6026899..6027618hg38UCSC Ensembl
Innerchr11:6048129..6048848hg19UCSC Ensembl
Innerchr11:6004705..6005424hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38720
hg19720
hg18720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975146
Supporting Variants
SamplesHGDP00665
Known GenesOR56A1
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)nssv1874476
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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