A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975202



Internal ID18610410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:73578012..73583804hg38UCSC Ensembl
Innerchr11:73289057..73294849hg19UCSC Ensembl
Innerchr11:72966705..72972497hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg385793
hg195793
hg185793
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1895423, nssv1895421, nssv1895427, nssv1895419, nssv1895418, nssv1895424, nssv1895426, nssv1895422, nssv1895420, nssv1895425
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM168A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975202
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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