A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999594



Internal ID21908937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31626597..31626863hg38UCSC Ensembl
chr5:31626704..31626970hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999594
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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