A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5414820



Internal ID194088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87912552..87918700hg38UCSC Ensembl
chr9:90527467..90533615hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386149
hg196149
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025634
Samples
Known GenesSPATA31C1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5414820
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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