A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916891



Internal ID22692110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31713725..31714077hg38UCSC Ensembl
chr8:31571241..31571593hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437099
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916891
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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