A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449155



Internal ID227400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102689536..102694238hg38UCSC Ensembl
chr3:102408380..102413082hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg384703
hg194703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937221
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449155
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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