A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550825



Internal ID20923966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40269399..40274657hg38UCSC Ensembl
chr20:38898039..38903297hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg385259
hg195259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4460n223
Supporting Variantsnssv18067562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550825
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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