A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534391



Internal ID20907752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1347394..1348889hg38UCSC Ensembl
chr20:1328038..1329533hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381496
hg191496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065814
Samples
Known GenesFKBP1A-SDCBP2, SDCBP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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