A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975157



Internal ID18610365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18260567..18263468hg38UCSC Ensembl
Innerchr11:18282114..18285015hg19UCSC Ensembl
Innerchr11:18238690..18241591hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382902
hg192902
hg182902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1877368, nssv1877370, nssv1877365, nssv1877373, nssv1877372, nssv1877374, nssv1877367, nssv1877366, nssv1877369, nssv1877371
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)nsv975157
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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