A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014455



Internal ID21923798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27593530..27594093hg38UCSC Ensembl
chr8:27451047..27451610hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014455
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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