A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240157



Internal ID22044767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112767124..112767124hg38UCSC Ensembl
chr9:115529404..115529404hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841335
Samples
Known GenesSNX30
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240157
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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