A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013876



Internal ID21923219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89909019..89909131hg38UCSC Ensembl
chr5:89204836..89204948hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013876
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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