A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593648



Internal ID21785691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129041534..129041601hg38UCSC Ensembl
chr8:130053780..130053847hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016645
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593648
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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