A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420272



Internal ID21077825
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 StatusM
Merged Variants
Supporting Variantsnssv18231799
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420272
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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