A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256288



Internal ID22060898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106535365..106535365hg38UCSC Ensembl
chr1:107077987..107077987hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256288
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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