A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538593



Internal ID21862948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14645038..14649559hg38UCSC Ensembl
chr3:14686545..14691066hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384522
hg194522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991805
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538593
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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