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nsv5402916

  • 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: 78 SVs from 26 studies. See in: genome view    
Submitted genomic47,628,369-47,628,420Question Mark
Overlapping variant regions from other studies: 78 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):47,649,921-47,649,972Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5402916Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1147,628,36947,628,420
nsv5402916RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1147,649,92147,649,972

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17045364alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17045364Submitted genomicNC_000011.10:g.476
28369_47628420ins2
47
GRCh38 (hg38)NC_000011.10Chr1147,628,36947,628,420
nssv17045364RemappedPerfectNC_000011.9:g.4764
9921_47649972ins24
7
GRCh37.p13First PassNC_000011.9Chr1147,649,92147,649,972

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)
nssv17045364<0.00116404
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