A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259375



Internal ID22063985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39207259..39207259hg38UCSC Ensembl
chr18:36787223..36787223hg19UCSC Ensembl
Cytoband18q12.2
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 Variantsnssv17849302
Samples
Known GenesLINC00669
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259375
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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