A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533052



Internal ID308949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44726173..44726407hg38UCSC Ensembl
chr20:43354814..43355048hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732570
Samples
Known GenesWISP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533052
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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