A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428129



Internal ID21085682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98518056..98518426hg38UCSC Ensembl
chr8:99530284..99530654hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173860
Samples
Known GenesSTK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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