A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551702



Internal ID20924834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52289507..52300163hg38UCSC Ensembl
chr20:50906046..50916702hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3810657
hg1910657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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