A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406494



Internal ID21064047
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 StatusM
Merged Variants
Supporting Variantsnssv18217399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406494
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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