A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6246821



Internal ID22051431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5668707..5668707hg38UCSC Ensembl
chr9:5668707..5668707hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17840506
Samples
Known GenesKIAA1432
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6246821
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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