A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859901



Internal ID22634836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42448999..42455511hg38UCSC Ensembl
chr9:44515608..44522120hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg386513
hg196513
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513412, nssv17513413, nssv17513414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859901
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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