A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1901801



Internal ID17877532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93858244..93864033hg38UCSC Ensembl
Innerchr11:93591410..93597199hg19UCSC Ensembl
Innerchr11:93231058..93236847hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385790
hg195790
hg185790
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975968
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)nssv1901801
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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