A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848487



Internal ID22623422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134162857..134167656hg38UCSC Ensembl
chr9:137027979..137032778hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511740
Samples
Known GenesRNU6ATAC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848487
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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