A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413232



Internal ID22471102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18964581..18964861hg38UCSC Ensembl
chr3:19006073..19006353hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897010
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413232
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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