A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249626



Internal ID22054236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111908088..111908088hg38UCSC Ensembl
chr13:112562402..112562402hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846018
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249626
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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