A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084348



Internal ID21993581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130084052..130084052hg38UCSC Ensembl
chr9:132846331..132846331hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584685
Samples
Known GenesGPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084348
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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