A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905767



Internal ID22680959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42532438..42532735hg38UCSC Ensembl
chr3:42573930..42574227hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421424
Samples
Known GenesVIPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905767
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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