A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112626



Internal ID21295892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:147512491..148041436hg38UCSC Ensembl
Innerchr6:147833627..148362572hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38528946
hg19528946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083757
Samplessample76
Known GenesSAMD5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112626
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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