A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168201



Internal ID20735241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32119345..32119715hg38UCSC Ensembl
chr8:31976861..31977231hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432539
Supporting Variants
Samples
Known GenesNRG1, NRG1-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168201
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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