A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608300



Internal ID20981371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162537921..162815336hg38UCSC Ensembl
chr6:162958953..163236368hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38277416
hg19277416
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216975
Samples
Known GenesPACRG, PARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608300
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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