A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1874703



Internal ID17879208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5967435..5968463hg38UCSC Ensembl
Innerchr11:5988665..5989693hg19UCSC Ensembl
Innerchr11:5945241..5946269hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381029
hg191029
hg181029
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv975875
Supporting Variants
SamplesHGDP01307
Known GenesOR56A5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1874703
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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