A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255912



Internal ID22060522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5279686..5279686hg38UCSC Ensembl
chr5:5279799..5279799hg19UCSC Ensembl
Cytoband5p15.32
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 Variantsnssv17857104
Samples
Known GenesADAMTS16
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255912
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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