A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231799



Internal ID20798839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84279119..84364734hg38UCSC Ensembl
chr8:85191354..85276969hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3885616
hg1985616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420272
Supporting Variants
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231799
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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