A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865412



Internal ID22640347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27203425..27205724hg38UCSC Ensembl
chr9:27203423..27205722hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512568
Samples
Known GenesTEK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865412
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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