A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256753



Internal ID22061363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79083059..79083059hg38UCSC Ensembl
chr6:79792776..79792776hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17857409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256753
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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