A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067396



Internal ID20634436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32506968..32509321hg38UCSC Ensembl
chr20:31094771..31097124hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg382354
hg192354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525031
Supporting Variants
Samples
Known GenesC20orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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