A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084493



Internal ID21993726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135549001..135549001hg38UCSC Ensembl
chr9:138440847..138440847hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578059
Samples
Known GenesOBP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084493
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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