A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532158



Internal ID20905519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:8099148..8101354hg38UCSC Ensembl
chr20:8079795..8082001hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg382207
hg192207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070538
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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