A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006209



Internal ID21915552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131573632..131576804hg38UCSC Ensembl
chr9:134449019..134452191hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg383173
hg193173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582570
Samples
Known GenesRAPGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006209
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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