A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1875964



Internal ID17746820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10153033..10160695hg38UCSC Ensembl
Innerchr11:10174580..10182242hg19UCSC Ensembl
Innerchr11:10131156..10138818hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387663
hg197663
hg187663
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv975150
Supporting Variants
SamplesHGDP00521
Known GenesSBF2
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)nssv1875964
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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