A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548071



Internal ID21872426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148849005..148849323hg38UCSC Ensembl
chr3:148566792..148567110hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991599
Supporting Variants
Samples
Known GenesCPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548071
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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