A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1876647



Internal ID17876538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11180427..11182386hg38UCSC Ensembl
Innerchr11:11201974..11203933hg19UCSC Ensembl
Innerchr11:11158550..11160509hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg381960
hg191960
hg181960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975883
Supporting Variants
SamplesHGDP01307
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)nssv1876647
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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