A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975166



Internal ID18610374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:35858949..35861957hg38UCSC Ensembl
Innerchr11:35880499..35883507hg19UCSC Ensembl
Innerchr11:35837075..35840083hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383009
hg193009
hg183009
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1881570, nssv1881572, nssv1881574, nssv1881571, nssv1881573, nssv1881577, nssv1881575, nssv1881569, nssv1881578, nssv1881576
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)nsv975166
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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