A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859387



Internal ID22634322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27221693..27225241hg38UCSC Ensembl
chr9:27221691..27225239hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg383549
hg193549
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512569
Samples
Known GenesTEK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859387
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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