A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018573



Internal ID21927916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108562388..108562504hg38UCSC Ensembl
chr5:107898089..107898205hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018573
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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