A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007545



Internal ID21916888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129018313..129018629hg38UCSC Ensembl
chr9:131780592..131780908hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584140
Samples
Known GenesSH3GLB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007545
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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