A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1871481



Internal ID17870560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1784090..1812954hg38UCSC Ensembl
Innerchr11:1805320..1834184hg19UCSC Ensembl
Innerchr11:1761896..1790760hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3828865
hg1928865
hg1828865
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975873
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)nssv1871481
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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