A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853989



Internal ID22628924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114832779..114836310hg38UCSC Ensembl
chr9:117595059..117598590hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg383532
hg193532
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510965, nssv17510964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853989
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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