A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447178



Internal ID225489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72467946..72477404hg38UCSC Ensembl
chr3:72517097..72526555hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg389459
hg199459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447178
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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