A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1907722



Internal ID17433922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124264837..124265945hg38UCSC Ensembl
Innerchr11:124134733..124135841hg19UCSC Ensembl
Innerchr11:123639943..123641051hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381109
hg191109
hg181109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv975993
Supporting Variants
SamplesHGDP00665
Known GenesOR8G1, OR8G5
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)nssv1907722
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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