A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983054



Internal ID18271562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93734512..93735802hg38UCSC Ensembl
Innerchr11:93467678..93468968hg19UCSC Ensembl
Innerchr11:93107326..93108616hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381291
hg191291
hg181291
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1901443, nssv1901447, nssv1901441, nssv1901444, nssv1901449, nssv1901446, nssv1901442, nssv1901440, nssv1901448, nssv1901445
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesSNORA40
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983054
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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