A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556292



Internal ID21880647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17246572..17246625hg38UCSC Ensembl
chr5:17246681..17246734hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999112
Supporting Variants
Samples
Known GenesBASP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556292
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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