A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901645



Internal ID22676797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4002099..4219002hg38UCSC Ensembl
chr3:4043783..4260686hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38216904
hg19216904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1438n209
Supporting Variantsnssv17417682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901645
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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