A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1906176



Internal ID17777442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119586171..119586671hg38UCSC Ensembl
Innerchr11:119456883..119457383hg19UCSC Ensembl
Innerchr11:118962093..118962593hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975232
Supporting Variants
SamplesHGDP00665
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)nssv1906176
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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