A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733048



Internal ID156714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53555733..53562204hg38UCSC Ensembl
chr20:52172272..52178743hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386472
hg196472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530184
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733048
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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