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nsv5559652

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 129 SVs from 29 studies. See in: genome view    
Submitted genomic73,243,097-73,243,097Question Mark
Overlapping variant regions from other studies: 129 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):74,108,814-74,108,814Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5559652Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr473,243,09773,243,097
nsv5559652RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr474,108,81474,108,814

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16952234mobile element insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16952234Submitted genomicNC_000004.12:g.732
43097_73243098ins1
90
GRCh38 (hg38)NC_000004.12Chr473,243,09773,243,097
nssv16952234RemappedPerfectNC_000004.11:g.741
08814_74108815ins1
90
GRCh37.p13First PassNC_000004.11Chr474,108,81474,108,814

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)
nssv16952234<0.00116404
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