A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068544



Internal ID20635584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62572082..62572951hg38UCSC Ensembl
chr20:61169289..61170158hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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