A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067973



Internal ID20635013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34891118..34891722hg38UCSC Ensembl
chr20:33478921..33479525hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527401
Supporting Variants
Samples
Known GenesACSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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