A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022718



Internal ID22084349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163702080..163725534hg38UCSC Ensembl
Outerchr6:163698216..163726185hg38UCSC Ensembl
Innerchr6:164123112..164146566hg19UCSC Ensembl
Outerchr6:164119248..164147217hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3827970
hg1927970
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156607
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022718
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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