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nsv5453373

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 116 SVs from 24 studies. See in: genome view    
Submitted genomic128,773,446-128,773,505Question Mark
Overlapping variant regions from other studies: 116 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):128,492,289-128,492,348Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5453373Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3128,773,446128,773,505
nsv5453373RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3128,492,289128,492,348

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16939836deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16939836Submitted genomicNC_000003.12:g.128
773446_128773505de
l
GRCh38 (hg38)NC_000003.12Chr3128,773,446128,773,505
nssv16939836RemappedPerfectNC_000003.11:g.128
492289_128492348de
l
GRCh37.p13First PassNC_000003.11Chr3128,492,289128,492,348

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)
nssv169398360.01676404
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