A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6242687



Internal ID22047297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75509271..75509271hg38UCSC Ensembl
chr18:73221226..73221226hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6242687
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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