A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257960



Internal ID22062570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98845936..98845936hg38UCSC Ensembl
chr9:101608218..101608218hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841106
Samples
Known GenesGALNT12
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257960
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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