A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6251405



Internal ID22056015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35203975..35203975hg38UCSC Ensembl
chr20:33791778..33791778hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17849953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6251405
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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