A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972072



Internal ID18607288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112180775..112185355hg38UCSC Ensembl
Innerchr11:112051498..112056078hg19UCSC Ensembl
Innerchr11:111556708..111561288hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg384581
hg194581
hg184581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1904700, nssv1904695, nssv1904694, nssv1904702, nssv1904696, nssv1904698, nssv1904697, nssv1904701, nssv1904699, nssv1904703
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesBCO2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972072
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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