A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854582



Internal ID22629517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2785935..2796312hg38UCSC Ensembl
chr9:2785935..2796312hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3810378
hg1910378
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512600
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854582
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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