A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983044



Internal ID18618238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75704125..75707513hg38UCSC Ensembl
Innerchr11:75415170..75418558hg19UCSC Ensembl
Innerchr11:75092818..75096206hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg383389
hg193389
hg183389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1896296, nssv1896292, nssv1896291, nssv1896293, nssv1896294, nssv1896290, nssv1896295, nssv1896299, nssv1896298, nssv1896297
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)nsv983044
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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