A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419109



Internal ID21076662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84884499..85034361hg38UCSC Ensembl
chr8:85796734..85946596hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38149863
hg19149863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172010
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419109
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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