A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910088



Internal ID22685298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133389206..133394827hg38UCSC Ensembl
chr9:136254990..136259954hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg385622
hg194965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448732
Samples
Known GenesC9orf96
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910088
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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