A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427096



Internal ID21084649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31637801..31641400hg38UCSC Ensembl
chr8:31495317..31498916hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228378
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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