A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863278



Internal ID22638213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32140892..32168474hg38UCSC Ensembl
chr8:31998408..32025990hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3827583
hg1927583
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509137
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863278
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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