A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156601



Internal ID22087002
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022708
Samples
Known GenesPACRG, PARK2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156601
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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