A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256594



Internal ID22061204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4490093..4490093hg38UCSC Ensembl
chr6:4490327..4490327hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256594
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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