A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983083



Internal ID18618277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107763..112509hg38UCSC Ensembl
Innerchr11:107763..112509hg19UCSC Ensembl
Innerchr11:97763..102509hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384747
hg194747
hg184747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2615310, nssv2614409, nssv2614412, nssv2614413, nssv2614414, nssv2615309, nssv2614411, nssv2614410, nssv2615311, nssv2614415
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983083
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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