A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429220



Internal ID21086773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106283014..106283424hg38UCSC Ensembl
chr8:107295242..107295652hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162379
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429220
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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