A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529162



Internal ID305196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40982068..40983307hg38UCSC Ensembl
chr20:39610708..39611947hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725973
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529162
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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