A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733490



Internal ID157156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61454261..61685924hg38UCSC Ensembl
chr20:60029317..60260980hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38231664
hg19231664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528683
Supporting Variants
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733490
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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