A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848450



Internal ID22623385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35646452..35647492hg38UCSC Ensembl
chr9:35646449..35647489hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381041
hg191041
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848450
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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