A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022681



Internal ID22084312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:134375877..134391529hg38UCSC Ensembl
Outerchr6:134375295..134397258hg38UCSC Ensembl
Innerchr6:134697015..134712667hg19UCSC Ensembl
Outerchr6:134696433..134718396hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3821964
hg1921964
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156587
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022681
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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