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nsv5422242

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 23 studies. See in: genome view    
Submitted genomic21,825,158-21,825,209Question Mark
Overlapping variant regions from other studies: 136 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):19,405,119-19,405,170Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5422242Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1821,825,15821,825,209
nsv5422242RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1819,405,11919,405,170

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17716561alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17716561Submitted genomicNC_000018.10:g.218
25158_21825209ins2
79
GRCh38 (hg38)NC_000018.10Chr1821,825,15821,825,209
nssv17716561RemappedPerfectNC_000018.9:g.1940
5119_19405170ins27
9
GRCh37.p13First PassNC_000018.9Chr1819,405,11919,405,170

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17716561<0.00116404
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