A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975187



Internal ID18610395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:57017909..57023612hg38UCSC Ensembl
Innerchr11:56785384..56791087hg19UCSC Ensembl
Innerchr11:56541960..56547663hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg385704
hg195704
hg185704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1890461, nssv1890465, nssv1890463, nssv1890460, nssv1890466, nssv1890459, nssv1890462, nssv1890464, nssv1890457, nssv1890458
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)nsv975187
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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