A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1880652



Internal ID17531324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:27581649..27582250hg38UCSC Ensembl
Innerchr11:27603196..27603797hg19UCSC Ensembl
Innerchr11:27559772..27560373hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38602
hg19602
hg18602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982998
Supporting Variants
SamplesHGDP01307
Known GenesBDNF-AS
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)nssv1880652
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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