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nsv4503724

  • 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: 17 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):47,726,330-47,726,330Question Mark
Overlapping variant regions from other studies: 17 SVs from 5 studies. See in: genome view    
Submitted genomic48,120,113-48,120,113Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4503724RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1247,726,33047,726,330
nsv4503724Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr1248,120,11348,120,113

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16001687alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16001687RemappedPerfectNC_000012.12:g.477
26330_47726331ins2
81
GRCh38.p12First PassNC_000012.12Chr1247,726,33047,726,330
nssv16001687Submitted genomicNC_000012.11:g.481
20113_48120114ins2
81
GRCh37.p13NC_000012.11Chr1248,120,11348,120,113

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)
nssv160016874.6e-005121694
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