A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6248893



Internal ID22053503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34058996..34058996hg38UCSC Ensembl
chr13:34633133..34633133hg19UCSC Ensembl
Cytoband13q13.2
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 Variantsnssv17845169
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6248893
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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