A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528683



Internal ID304730
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 StatusM
Merged Variants
Supporting Variantsnssv17733490
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528683
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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