A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391180



Internal ID22449050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63956453..63956514hg38UCSC Ensembl
chr20:62587806..62587867hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965920
Supporting Variants
Samples
Known GenesUCKL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391180
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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