A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901793



Internal ID22676946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4021635..4201447hg38UCSC Ensembl
chr3:4063319..4243131hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38179813
hg19179813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1438n209
Supporting Variantsnssv17417964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901793
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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