A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156444



Internal ID22086845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:327531..379015hg38UCSC Ensembl
Outerchr6:323576..381149hg38UCSC Ensembl
Innerchr6:327531..379015hg19UCSC Ensembl
Outerchr6:323576..381149hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3857574
hg1957574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv242n97
Supporting Variantsnssv4018297
Samples
Known GenesDUSP22
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156444
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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