A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1898640



Internal ID17534070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85857855..85859095hg38UCSC Ensembl
Innerchr11:85568898..85570138hg19UCSC Ensembl
Innerchr11:85246546..85247786hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381241
hg191241
hg181241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975957
Supporting Variants
SamplesHGDP01307
Known GenesCCDC83
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)nssv1898640
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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