A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004546



Internal ID21913889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108559038..108559165hg38UCSC Ensembl
chr5:107894739..107894866hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004546
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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