A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449727



Internal ID227955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142727909..142727976hg38UCSC Ensembl
chr3:142446751..142446818hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938894
Samples
Known GenesTRPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449727
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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