A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520539



Internal ID20893900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10822901..10952100hg38UCSC Ensembl
chr20:10803549..10932748hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38129200
hg19129200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520539
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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