A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446871



Internal ID225189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140074311..140074367hg38UCSC Ensembl
chr3:139793153..139793209hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938841
Samples
Known GenesCLSTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446871
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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