A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216973



Internal ID20784013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162445491..162922097hg38UCSC Ensembl
chr6:162866523..163343129hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38476607
hg19476607
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613135
Supporting Variants
Samples
Known GenesPACRG, PARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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