A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983211



Internal ID18618405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:110000585..110028507hg38UCSC Ensembl
Innerchr11:109871311..109899233hg19UCSC Ensembl
Innerchr11:109376521..109404443hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3827923
hg1927923
hg1827923
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763444
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983211
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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