A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257229



Internal ID22061839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135109879..135109879hg38UCSC Ensembl
chr6:135431017..135431017hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257229
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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