A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413402



Internal ID22471272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194721279..194723565hg38UCSC Ensembl
chr3:194442008..194444294hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382287
hg192287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892477
Supporting Variants
Samples
Known GenesLOC100507391
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413402
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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