A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891549



Internal ID22666589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99501864..99502111hg38UCSC Ensembl
chr3:99220708..99220955hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891549
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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