A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446123



Internal ID224452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63816810..63818257hg38UCSC Ensembl
chr3:63802486..63803933hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381448
hg191448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446123
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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