A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850507



Internal ID22625442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42761140..42776222hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3815083
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513468, nssv17513469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850507
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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