A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527087



Internal ID20900448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16579901..16613700hg38UCSC Ensembl
chr20:16560546..16594345hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3833800
hg1933800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527087
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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