A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1875916



Internal ID17523318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6683474..6694742hg38UCSC Ensembl
Innerchr11:6704705..6715973hg19UCSC Ensembl
Innerchr11:6661281..6672549hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811269
hg1911269
hg1811269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975878
Supporting Variants
SamplesHGDP01284
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)nssv1875916
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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