A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15179744



Internal ID21318540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52898369..52898489hg38UCSC Ensembl
chr3:52932385..52932505hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3940363
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15179744
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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