A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240193



Internal ID22044803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118311656..118311656hg38UCSC Ensembl
chr9:121073934..121073934hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240193
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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