A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6258926



Internal ID22063536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59370800..59370800hg38UCSC Ensembl
chr14:59837518..59837518hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846087
Samples
Known GenesDAAM1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6258926
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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