A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423773



Internal ID22481643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152589134..152589366hg38UCSC Ensembl
chr3:152306923..152307155hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898068
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423773
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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