A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003219



Internal ID21912562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28418214..28418280hg38UCSC Ensembl
chr8:28275731..28275797hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563090
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003219
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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