A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000801



Internal ID21910144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32302654..32302866hg38UCSC Ensembl
chr8:32160170..32160382hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558783
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000801
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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