A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859388



Internal ID22634323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42473406..42491778hg38UCSC Ensembl
chr9:44479341..44497713hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3818373
hg1918373
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2115n209
Supporting Variantsnssv17513426, nssv17513427, nssv17513425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859388
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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