A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028499



Internal ID21937842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:46409534..46420616hg38UCSC Ensembl
chr15:46701732..46712814hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3811083
hg1911083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599067
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028499
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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