A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067124



Internal ID20634164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16321601..16325700hg38UCSC Ensembl
chr20:16302246..16306345hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522950
Supporting Variants
Samples
Known GenesKIF16B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067124
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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