A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975229



Internal ID18610437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:115948809..115953460hg38UCSC Ensembl
Innerchr11:115819527..115824178hg19UCSC Ensembl
Innerchr11:115324737..115329388hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg384652
hg194652
hg184652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1904899, nssv1904897, nssv1904900, nssv1904901, nssv1904905, nssv1904904, nssv1904898, nssv1904902, nssv1904906, nssv1904903
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)nsv975229
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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