A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249616



Internal ID22054226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110079479..110079479hg38UCSC Ensembl
chr13:110731826..110731826hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846008
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249616
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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