A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000558



Internal ID21909901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21551773..21551887hg38UCSC Ensembl
chr6:21552004..21552118hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000558
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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