A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983067



Internal ID18271575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119015730..119018887hg38UCSC Ensembl
Innerchr11:118886440..118889597hg19UCSC Ensembl
Innerchr11:118391650..118394807hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383158
hg193158
hg183158
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1906079, nssv1906077, nssv1906071, nssv1906078, nssv1906073, nssv1906075, nssv1906074, nssv1906080, nssv1906072, nssv1906076
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCDC84, RPS25, TRAPPC4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983067
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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