A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975883



Internal ID18611090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11180427..11182386hg38UCSC Ensembl
Innerchr11:11201974..11203933hg19UCSC Ensembl
Innerchr11:11158550..11160509hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg381960
hg191960
hg181960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1876648, nssv1876653, nssv1876652, nssv1876650, nssv1876656, nssv1876649, nssv1876654, nssv1876647, nssv1876655, nssv1876651
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)nsv975883
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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