A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419645



Internal ID21077198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18182361..18733199hg38UCSC Ensembl
chr8:18039870..18590709hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38550839
hg19550840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225970
Samples
Known GenesNAT1, NAT2, PSD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419645
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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