A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730342



Internal ID154008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2696338..2697420hg38UCSC Ensembl
chr20:2676984..2678066hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533033
Supporting Variants
Samples
Known GenesEBF4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730342
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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