A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216756



Internal ID20783796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162124663..162739694hg38UCSC Ensembl
chr6:162545695..163160726hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38615032
hg19615032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607661
Supporting Variants
Samples
Known GenesPACRG, PARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216756
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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