A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4018301



Internal ID22079932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:342906..378703hg38UCSC Ensembl
Outerchr6:336809..378970hg38UCSC Ensembl
Innerchr6:342906..378703hg19UCSC Ensembl
Outerchr6:336809..378970hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3842162
hg1942162
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156447
Supporting Variants
Samples
Known GenesDUSP22
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4018301
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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