A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866741



Internal ID22641676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27194071..27203824hg38UCSC Ensembl
chr9:27194069..27203822hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg389754
hg199754
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512567
Samples
Known GenesTEK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866741
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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