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nsv5497780

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:634

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 30 studies. See in: genome view    
Submitted genomic122,886,474-122,887,107Question Mark
Overlapping variant regions from other studies: 113 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):123,371,021-123,371,654Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5497780Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12122,886,474122,887,107
nsv5497780RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12123,371,021123,371,654

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17690766deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17690766Submitted genomicNC_000012.12:g.122
886474_122887107de
l
GRCh38 (hg38)NC_000012.12Chr12122,886,474122,887,107
nssv17690766RemappedPerfectNC_000012.11:g.123
371021_123371654de
l
GRCh37.p13First PassNC_000012.11Chr12123,371,021123,371,654

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)
nssv17690766<0.00126404
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