A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852287



Internal ID22627222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20958299..20967449hg38UCSC Ensembl
chr9:20958298..20967448hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg389151
hg199151
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2082n209
Supporting Variantsnssv17512214
Samples
Known GenesFOCAD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852287
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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