A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975222



Internal ID18610430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:104949314..104949814hg38UCSC Ensembl
Innerchr11:104820041..104820541hg19UCSC Ensembl
Innerchr11:104325251..104325751hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1901495, nssv1901497, nssv1901492, nssv1901498, nssv1901494, nssv1901496, nssv1901493, nssv1901490, nssv1901491, nssv1901489
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCASP4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975222
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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