A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014877



Internal ID22076508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41460614..41465336hg38UCSC Ensembl
Outerchr21:41455551..41465764hg38UCSC Ensembl
Innerchr21:42832541..42837263hg19UCSC Ensembl
Outerchr21:42827478..42837691hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3810214
hg1910214
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155741
Supporting Variants
Samples
Known GenesMX1, TMPRSS2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014877
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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