A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241720



Internal ID22046330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96467062..96467062hg38UCSC Ensembl
chr14:96933399..96933399hg19UCSC Ensembl
Cytoband14q32.2
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 Variantsnssv17846554
Samples
Known GenesAK7
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241720
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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