A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975981



Internal ID18264502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:114582666..114583939hg38UCSC Ensembl
Innerchr11:114453388..114454661hg19UCSC Ensembl
Innerchr11:113958598..113959871hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg381274
hg191274
hg181274
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1903689, nssv1903684, nssv1903688, nssv1903686, nssv1903681, nssv1903685, nssv1903680, nssv1903683, nssv1903687, nssv1903682
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesNXPE4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975981
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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