A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449148



Internal ID227394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180943734..180946921hg38UCSC Ensembl
chr3:180661522..180664709hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg383188
hg193188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944678
Samples
Known GenesFXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449148
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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