A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902597



Internal ID22677757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4041955..4125629hg38UCSC Ensembl
chr3:4083639..4167313hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3883675
hg1983675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1439n209
Supporting Variantsnssv17429262
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902597
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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