A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422152



Internal ID22480022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16515084..16521702hg38UCSC Ensembl
chr3:16556591..16563209hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg386619
hg196619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896690
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422152
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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