A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975965



Internal ID18611172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90200362..90202949hg38UCSC Ensembl
Innerchr11:89933530..89936117hg19UCSC Ensembl
Innerchr11:89573178..89575765hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg382588
hg192588
hg182588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1899788, nssv1899789, nssv1899792, nssv1899793, nssv1899796, nssv1899794, nssv1899791, nssv1899790, nssv1899795, nssv1899787
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCHORDC1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975965
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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