A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901258



Internal ID22676407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18194334..18207647hg38UCSC Ensembl
chr3:18235826..18249139hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3813314
hg1913314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426199
Samples
Known GenesLOC339862
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901258
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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