A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1880558



Internal ID17829675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:26588421..26598720hg38UCSC Ensembl
Innerchr11:26609968..26620267hg19UCSC Ensembl
Innerchr11:26566544..26576843hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg3810300
hg1910300
hg1810300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975163
Supporting Variants
SamplesHGDP00998
Known GenesANO3
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)nssv1880558
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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