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nsv5512120

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,245

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 339 SVs from 39 studies. See in: genome view    
Submitted genomic43,075,547-43,078,791Question Mark
Overlapping variant regions from other studies: 339 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):43,649,683-43,652,927Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5512120Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1343,075,54743,078,791
nsv5512120RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1343,649,68343,652,927

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17687271deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17687271Submitted genomicNC_000013.11:g.430
75547_43078791del
GRCh38 (hg38)NC_000013.11Chr1343,075,54743,078,791
nssv17687271RemappedPerfectNC_000013.10:g.436
49683_43652927del
GRCh37.p13First PassNC_000013.10Chr1343,649,68343,652,927

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)
nssv17687271<0.00116404
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