A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975932



Internal ID18611139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58242275..58243086hg38UCSC Ensembl
Innerchr11:58009747..58010558hg19UCSC Ensembl
Innerchr11:57766323..57767134hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38812
hg19812
hg18812
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1890894, nssv1890887, nssv1890889, nssv1890888, nssv1890885, nssv1890886, nssv1890891, nssv1890890, nssv1890893, nssv1890892
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975932
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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