A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009042



Internal ID21918385
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 StatusM
Merged Variants
Supporting Variantsnssv17582083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009042
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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