A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860288



Internal ID22635223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133391606..133394847hg38UCSC Ensembl
chr9:136257382..136259974hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg383242
hg192593
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511693
Samples
Known GenesC9orf96
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860288
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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