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nsv5476325

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:62

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 27 studies. See in: genome view    
Submitted genomic107,582,438-107,582,499Question Mark
Overlapping variant regions from other studies: 114 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):107,222,883-107,222,944Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5476325Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7107,582,438107,582,499
nsv5476325RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7107,222,883107,222,944

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17004037deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17004037Submitted genomicNC_000007.14:g.107
582438_107582499de
l
GRCh38 (hg38)NC_000007.14Chr7107,582,438107,582,499
nssv17004037RemappedPerfectNC_000007.13:g.107
222883_107222944de
l
GRCh37.p13First PassNC_000007.13Chr7107,222,883107,222,944

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)
nssv17004037<0.00116404
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