A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1896196



Internal ID17830761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75075277..75088699hg38UCSC Ensembl
Innerchr11:74786322..74799744hg19UCSC Ensembl
Innerchr11:74463970..74477392hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3813423
hg1913423
hg1813423
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975203
Supporting Variants
SamplesHGDP00998
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)nssv1896196
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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