nsv5928694

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 128 SVs from 32 studies. See in: genome view    
Submitted genomic124,817,046-124,817,099Question Mark
Overlapping variant regions from other studies: 128 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):125,301,592-125,301,645Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5928694Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12124,817,046124,817,099
nsv5928694RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12125,301,592125,301,645

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17363121deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17363121Submitted genomicNC_000012.12:g.124
817046_124817099de
l
GRCh38 (hg38)NC_000012.12Chr12124,817,046124,817,099
nssv17363121RemappedPerfectNC_000012.11:g.125
301592_125301645de
l
GRCh37.p13First PassNC_000012.11Chr12125,301,592125,301,645

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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