A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975905



Internal ID18611112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37725858..37726358hg38UCSC Ensembl
Innerchr11:37747408..37747908hg19UCSC Ensembl
Innerchr11:37703984..37704484hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1882751, nssv1882750, nssv1882749, nssv1882757, nssv1882756, nssv1882753, nssv1882752, nssv1882758, nssv1882754, nssv1882755
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)nsv975905
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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