A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421217



Internal ID21078770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98054981..98063848hg38UCSC Ensembl
chr8:99067209..99076076hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg388868
hg198868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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