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nsv5486060

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:66

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 20 studies. See in: genome view    
Submitted genomic107,772,401-107,772,466Question Mark
Overlapping variant regions from other studies: 97 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):107,412,846-107,412,911Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5486060Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7107,772,401107,772,466
nsv5486060RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7107,412,846107,412,911

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17004051deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17004051Submitted genomicNC_000007.14:g.107
772401_107772466de
l
GRCh38 (hg38)NC_000007.14Chr7107,772,401107,772,466
nssv17004051RemappedPerfectNC_000007.13:g.107
412846_107412911de
l
GRCh37.p13First PassNC_000007.13Chr7107,412,846107,412,911

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)
nssv17004051<0.00116404
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