A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865425



Internal ID22640360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128363722..128367285hg38UCSC Ensembl
chr9:131126001..131129564hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383564
hg193564
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865425
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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