A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156588



Internal ID22086989
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022682
Samples
Known GenesMYB
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156588
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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