A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860745



Internal ID22635680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43110680..43113171hg38UCSC Ensembl
chr9:42872067..42874548hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg382492
hg192482
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513589
Samples
Known GenesAQP7P3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860745
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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