A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902661



Internal ID22677821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63750599..63752713hg38UCSC Ensembl
chr3:63736275..63738389hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382115
hg192115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410838
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902661
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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