A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972070



Internal ID18607286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:108690205..108690811hg38UCSC Ensembl
Innerchr11:108560932..108561538hg19UCSC Ensembl
Innerchr11:108066142..108066748hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38607
hg19607
hg18607
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1904161, nssv1904166, nssv1904159, nssv1904164, nssv1904162, nssv1904158, nssv1904163, nssv1904160, nssv1904165, nssv1904167
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDDX10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972070
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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