A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028566



Internal ID21937909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58226903..58292668hg38UCSC Ensembl
chr15:58519102..58584867hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3865766
hg1965766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028566
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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