A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17844943



Internal ID22028586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44095016..44095016hg38UCSC Ensembl
chr13:44669152..44669152hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17844943
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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