A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586771



Internal ID21778814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65520744..65520848hg38UCSC Ensembl
chr8:66432979..66433083hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007151
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586771
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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