A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972073



Internal ID18260603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112234304..112236104hg38UCSC Ensembl
Innerchr11:112105027..112106827hg19UCSC Ensembl
Innerchr11:111610237..111612037hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg381801
hg191801
hg181801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1905529, nssv1905533, nssv1905536, nssv1905534, nssv1905537, nssv1905532, nssv1905538, nssv1905535, nssv1905530, nssv1905531
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972073
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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