A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022702



Internal ID22084333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154642532..154650798hg38UCSC Ensembl
Outerchr6:154639748..154654106hg38UCSC Ensembl
Innerchr6:154963666..154971932hg19UCSC Ensembl
Outerchr6:154960882..154975240hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3814359
hg1914359
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156596
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022702
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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