A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015960



Internal ID21925303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89404898..89404995hg38UCSC Ensembl
chr9:92019813..92019910hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592086
Samples
Known GenesSEMA4D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015960
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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