A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156584



Internal ID22086985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125258338..125266277hg38UCSC Ensembl
Outerchr6:125255285..125266815hg38UCSC Ensembl
Innerchr6:125579484..125587423hg19UCSC Ensembl
Outerchr6:125576431..125587961hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3811531
hg1911531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022634
Samples
Known GenesTPD52L1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156584
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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