A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018295



Internal ID22079926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:327531..366333hg38UCSC Ensembl
Outerchr6:323576..373453hg38UCSC Ensembl
Innerchr6:327531..366333hg19UCSC Ensembl
Outerchr6:323576..373453hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3849878
hg1949878
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156442
Supporting Variants
Samples
Known GenesDUSP22
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018295
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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