A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427104



Internal ID21084657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31861379..31883909hg38UCSC Ensembl
chr8:31718895..31741425hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3822531
hg1922531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220004
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427104
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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