A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423620



Internal ID22481490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20970425..20974172hg38UCSC Ensembl
chr3:21011917..21015664hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg383748
hg193748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896938
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423620
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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