A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421424



Internal ID22479294
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 StatusS
Merged Variantsnsv5905767
Supporting Variants
Samples
Known GenesVIPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421424
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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