A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904215



Internal ID22679391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62917630..62933936hg38UCSC Ensembl
chr3:62903305..62919611hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3816307
hg1916307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904215
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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