A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975958



Internal ID18611165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86195689..86196905hg38UCSC Ensembl
Innerchr11:85906731..85907947hg19UCSC Ensembl
Innerchr11:85584379..85585595hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg381217
hg191217
hg181217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1898746, nssv1898744, nssv1898741, nssv1898742, nssv1898737, nssv1898738, nssv1898740, nssv1898743, nssv1898745, nssv1898739
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)nsv975958
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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