A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068359



Internal ID20635399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45744145..45758779hg38UCSC Ensembl
chr20:44372784..44387418hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3814635
hg1914635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00121


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