A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900737



Internal ID22675882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23943009..23943484hg38UCSC Ensembl
chr3:23984500..23984975hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900737
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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