A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241726



Internal ID22046336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97940304..97940304hg38UCSC Ensembl
chr14:98406641..98406641hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846560
Samples
Known GenesC14orf64
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241726
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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