A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982983



Internal ID18618177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9958795..9959795hg38UCSC Ensembl
Innerchr11:9980342..9981342hg19UCSC Ensembl
Innerchr11:9936918..9937918hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1875077, nssv1875075, nssv1875076, nssv1875074, nssv1875079, nssv1875083, nssv1875082, nssv1875078, nssv1875080, nssv1875081
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSBF2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982983
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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