A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847882



Internal ID22622817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125760859..125764217hg38UCSC Ensembl
chr9:128523138..128526496hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg383359
hg193359
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511374
Samples
Known GenesPBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847882
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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