A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849499



Internal ID22624434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43086800..43089187hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382388
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513583, nssv17513584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849499
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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