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nsv5416162

  • 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: 77 SVs from 20 studies. See in: genome view    
Submitted genomic52,011,505-52,011,556Question Mark
Overlapping variant regions from other studies: 77 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):52,478,223-52,478,274Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5416162Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1452,011,50552,011,556
nsv5416162RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1452,478,22352,478,274

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17696206alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17696206Submitted genomicNC_000014.9:g.5201
1505_52011556ins27
8
GRCh38 (hg38)NC_000014.9Chr1452,011,50552,011,556
nssv17696206RemappedPerfectNC_000014.8:g.5247
8223_52478274ins27
8
GRCh37.p13First PassNC_000014.8Chr1452,478,22352,478,274

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)
nssv17696206<0.00156404
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