A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556509



Internal ID21880864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107406263..107406488hg38UCSC Ensembl
chr3:107125110..107125335hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990954
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556509
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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