A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6253384



Internal ID22057994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217075602..217075602hg38UCSC Ensembl
chr2:217940325..217940325hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17854017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6253384
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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