A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855038



Internal ID22629973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32158246..32191408hg38UCSC Ensembl
chr8:32015762..32048924hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3833163
hg1933163
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505952
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855038
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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