A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1880132



Internal ID17763545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31274229..31283848hg38UCSC Ensembl
Innerchr11:31295776..31305395hg19UCSC Ensembl
Innerchr11:31252352..31261971hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg389620
hg199620
hg189620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975898
Supporting Variants
SamplesHGDP00542
Known GenesDCDC1
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)nssv1880132
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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