A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165958



Internal ID20732998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32674454..32675227hg38UCSC Ensembl
chr8:32531973..32532746hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38774
hg19774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427935
Supporting Variants
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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