A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520168



Internal ID20893529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6397281..6398002hg38UCSC Ensembl
chr20:6377928..6378649hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070280
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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