A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020087



Internal ID21929430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45646163..45646705hg38UCSC Ensembl
chr6:45613900..45614442hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020087
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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