A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536658



Internal ID21861013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4198457..4240465hg38UCSC Ensembl
chr3:4240141..4282149hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3842009
hg1942009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993378
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536658
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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