A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018299



Internal ID22079930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:327531..381149hg38UCSC Ensembl
Outerchr6:323576..382559hg38UCSC Ensembl
Innerchr6:327531..381149hg19UCSC Ensembl
Outerchr6:323576..382559hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3858984
hg1958984
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156445
Supporting Variants
Samples
Known GenesDUSP22
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018299
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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