A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521869



Internal ID20895230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11328642..11330919hg38UCSC Ensembl
chr20:11309290..11311567hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg382278
hg192278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521869
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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