A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218469



Internal ID20785509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32201353..32229514hg38UCSC Ensembl
chr8:32058869..32087030hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3828162
hg1928162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417464
Supporting Variants
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218469
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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