A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862058



Internal ID22636993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25937876..25948979hg38UCSC Ensembl
chr9:25937874..25948977hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3811104
hg1911104
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862058
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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