A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012096



Internal ID21921439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97612339..97615093hg38UCSC Ensembl
chr8:98624567..98627321hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382755
hg192755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012096
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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