A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451449



Internal ID229631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14492604..14493389hg38UCSC Ensembl
chr3:14534112..14534897hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930156
Samples
Known GenesGRIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451449
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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