A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733472



Internal ID157138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61312138..61312281hg38UCSC Ensembl
chr20:59887194..59887337hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526467
Supporting Variants
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733472
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.005151


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer