A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1874376



Internal ID17737984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5993042..5995541hg38UCSC Ensembl
Innerchr11:6014272..6016771hg19UCSC Ensembl
Innerchr11:5970848..5973347hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382500
hg192500
hg182500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982978
Supporting Variants
SamplesHGDP00456
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)nssv1874376
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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