A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530986



Internal ID306952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36876521..36877079hg38UCSC Ensembl
chr20:35504924..35505482hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732223
Samples
Known GenesTLDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530986
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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