A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582083



Internal ID21774126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100445964..100446044hg38UCSC Ensembl
chr8:101458192..101458272hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582083
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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