A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848762



Internal ID22623697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26441777..26459302hg38UCSC Ensembl
chr9:26441775..26459300hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3817526
hg1917526
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848762
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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