A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859902



Internal ID22634837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42847637..42857128hg38UCSC Ensembl
chr9:44113991..44123482hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg389492
hg199492
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513498, nssv17513499
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859902
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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