A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257149



Internal ID22061759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125772809..125772809hg38UCSC Ensembl
chr6:126093955..126093955hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257149
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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