A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222106



Internal ID20789146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83228651..83249100hg38UCSC Ensembl
chr6:83938370..83958819hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg3820450
hg1920450
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403697
Supporting Variants
Samples
Known GenesME1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222106
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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