A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009380



Internal ID73887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32655319..32655944hg38UCSC Ensembl
chr8:32512838..32513463hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482072
Supporting Variants
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009380
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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