A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975225



Internal ID18610433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:109980904..109982864hg38UCSC Ensembl
Innerchr11:109851630..109853590hg19UCSC Ensembl
Innerchr11:109356840..109358800hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381961
hg191961
hg181961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1904366, nssv1904368, nssv1904364, nssv1904369, nssv1904371, nssv1904370, nssv1904367, nssv1904365, nssv1904372, nssv1904363
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)nsv975225
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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