A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424468



Internal ID22482338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193721259..193725592hg38UCSC Ensembl
chr3:193439048..193443381hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg384334
hg194334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424468
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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