A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240251



Internal ID22044861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128694734..128694734hg38UCSC Ensembl
chr9:131457013..131457013hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842002
Samples
Known GenesSET
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240251
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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