A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417583



Internal ID21075136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32643304..32643774hg38UCSC Ensembl
chr8:32500823..32501293hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165954
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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