A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022682



Internal ID22084313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135210501..135216114hg38UCSC Ensembl
Outerchr6:135210313..135216614hg38UCSC Ensembl
Innerchr6:135531639..135537252hg19UCSC Ensembl
Outerchr6:135531451..135537752hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg386302
hg196302
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156588
Supporting Variants
Samples
Known GenesMYB
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022682
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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