A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022708



Internal ID22084339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162157489..162780824hg38UCSC Ensembl
Outerchr6:162154482..162786150hg38UCSC Ensembl
Innerchr6:162578521..163201856hg19UCSC Ensembl
Outerchr6:162575514..163207182hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38631669
hg19631669
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156601
Supporting Variants
Samples
Known GenesPACRG, PARK2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022708
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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