A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848198



Internal ID22623133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116134898..116139600hg38UCSC Ensembl
chr9:118897177..118901879hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg384703
hg194703
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848198
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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