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nsv5562368

  • 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: 224 SVs from 31 studies. See in: genome view    
Submitted genomic98,795,108-98,795,159Question Mark
Overlapping variant regions from other studies: 224 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):99,338,337-99,338,388Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5562368Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1598,795,10898,795,159
nsv5562368RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1599,338,33799,338,388

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17705241sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17705241Submitted genomicNC_000015.10:g.987
95108_98795159ins1
289
GRCh38 (hg38)NC_000015.10Chr1598,795,10898,795,159
nssv17705241RemappedPerfectNC_000015.9:g.9933
8337_99338388ins12
89
GRCh37.p13First PassNC_000015.9Chr1599,338,33799,338,388

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)
nssv17705241<0.00136404
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