A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426979



Internal ID21084532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98709241..98717445hg38UCSC Ensembl
chr8:99721469..99729673hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg388205
hg198205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173867
Samples
Known GenesSTK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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