A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848479



Internal ID22623414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131274235..131280033hg38UCSC Ensembl
chr9:134149622..134155420hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg385799
hg195799
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511577
Samples
Known GenesFAM78A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848479
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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