A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975226



Internal ID18610434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:110294066..110297011hg38UCSC Ensembl
Innerchr11:110164791..110167736hg19UCSC Ensembl
Innerchr11:109670001..109672946hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382946
hg192946
hg182946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1905093, nssv1905089, nssv1905090, nssv1905087, nssv1905085, nssv1905094, nssv1905092, nssv1905091, nssv1905086, nssv1905088
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRDX
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975226
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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