A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589126



Internal ID21781169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142975283..142975704hg38UCSC Ensembl
chr8:144056700..144057121hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589126
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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