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nsv5502894

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,367

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 35 studies. See in: genome view    
Submitted genomic120,306,313-120,307,679Question Mark
Overlapping variant regions from other studies: 114 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):120,744,116-120,745,482Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5502894Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12120,306,313120,307,679
nsv5502894RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12120,744,116120,745,482

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684893deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684893Submitted genomicNC_000012.12:g.120
306313_120307679de
l
GRCh38 (hg38)NC_000012.12Chr12120,306,313120,307,679
nssv17684893RemappedPerfectNC_000012.11:g.120
744116_120745482de
l
GRCh37.p13First PassNC_000012.11Chr12120,744,116120,745,482

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)
nssv17684893<0.00156404
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