A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6253296



Internal ID22057906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207589636..207589636hg38UCSC Ensembl
chr2:208454360..208454360hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851123
Samples
Known GenesCREB1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6253296
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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