A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853882



Internal ID22628817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29175532..29187637hg38UCSC Ensembl
chr9:29175530..29187635hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3812106
hg1912106
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512688
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853882
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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