A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235369



Internal ID20802409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32181272..32229367hg38UCSC Ensembl
chr8:32038788..32086883hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3848096
hg1948096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424797
Supporting Variants
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235369
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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