A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900263



Internal ID22675403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44421822..44424236hg38UCSC Ensembl
chr3:44463314..44465728hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382415
hg192415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900263
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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