A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6251212



Internal ID22055822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7085475..7085475hg38UCSC Ensembl
chr20:7066122..7066122hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6251212
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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