A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733531



Internal ID157197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61941897..61959116hg38UCSC Ensembl
chr20:60516953..60534172hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3817220
hg1917220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520198
Supporting Variants
Samples
Known GenesMIR1257
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733531
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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