A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156443



Internal ID22086844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:327531..373453hg38UCSC Ensembl
Outerchr6:323576..375277hg38UCSC Ensembl
Innerchr6:327531..373453hg19UCSC Ensembl
Outerchr6:323576..375277hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3851702
hg1951702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv242n97
Supporting Variantsnssv4018296
Samples
Known GenesDUSP22
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156443
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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