A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292717



Internal ID20501935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17246593..17246645hg38UCSC Ensembl
chr5:17246702..17246754hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737081
Supporting Variants
Samples
Known GenesBASP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292717
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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