A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422129



Internal ID21079682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27901733..27902621hg38UCSC Ensembl
chr8:27759250..27760138hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166131
Samples
Known GenesSCARA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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