A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528735



Internal ID304779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63960292..63960633hg38UCSC Ensembl
chr20:62591645..62591986hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733709
Samples
Known GenesZNF512B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528735
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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