A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156573



Internal ID22086974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112443136..112520206hg38UCSC Ensembl
Outerchr6:112438967..112524523hg38UCSC Ensembl
Innerchr6:112764338..112841408hg19UCSC Ensembl
Outerchr6:112760169..112845725hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3885557
hg1985557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022623
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156573
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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