A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434506



Internal ID21092059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18318711..18402598hg38UCSC Ensembl
chr8:18176220..18260108hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3883888
hg1983889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236792
Samples
Known GenesNAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434506
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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