A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861512



Internal ID22636447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18083815..18095678hg38UCSC Ensembl
chr9:18083813..18095676hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3811864
hg1911864
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512105
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861512
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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