A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848987



Internal ID22623922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1809306..1812615hg38UCSC Ensembl
chr9:1809306..1812615hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg383310
hg193310
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848987
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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