A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1890560



Internal ID17760707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:57574247..57577057hg38UCSC Ensembl
Innerchr11:57341720..57344530hg19UCSC Ensembl
Innerchr11:57098296..57101106hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382811
hg192811
hg182811
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983025
Supporting Variants
SamplesHGDP00542
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)nssv1890560
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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