A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067899



Internal ID20634939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54030301..54040200hg38UCSC Ensembl
chr20:52646840..52656739hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541639
Supporting Variants
Samples
Known GenesBCAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02365


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