A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217399



Internal ID20784439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18697022..19117672hg38UCSC Ensembl
chr6:18697253..19117903hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38420651
hg19420651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406494
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217399
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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