A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515748



Internal ID292226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35033485..35034152hg38UCSC Ensembl
chr20:33621288..33621955hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732137
Samples
Known GenesTRPC4AP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515748
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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