A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737081



Internal ID20513038
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 StatusM
Merged Variants
Supporting Variantsnssv16292717
Samples
Known GenesBASP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737081
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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