A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447297



Internal ID225606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45684682..45684739hg38UCSC Ensembl
chr3:45726174..45726231hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933258
Samples
Known GenesLIMD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447297
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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