A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866068



Internal ID22641003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42840270..42843235hg38UCSC Ensembl
chr9:44127884..44130849hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg382966
hg192966
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513490, nssv17513491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866068
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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