A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432617



Internal ID21090170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31589818..32245704hg38UCSC Ensembl
chr8:31447334..32103220hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38655887
hg19655887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236891
Samples
Known GenesNRG1, NRG1-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432617
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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