A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6246552



Internal ID22051162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115899108..115899108hg38UCSC Ensembl
chr8:116911333..116911333hg19UCSC Ensembl
Cytoband8q23.3
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 Variantsnssv17840029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6246552
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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