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nsv5205376

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:322

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 180 SVs from 58 studies. See in: genome view    
Submitted genomic122,525,799-122,526,120Question Mark
Overlapping variant regions from other studies: 180 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):123,010,346-123,010,667Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5205376Submitted genomicGRCh38.p13Primary AssemblyNC_000012.12Chr12122,525,799122,526,120
nsv5205376RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12123,010,346123,010,667

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16741823alu deletionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16741823Submitted genomicNC_000012.12:g.122
525799_122526120de
l
GRCh38.p13NC_000012.12Chr12122,525,799122,526,120
nssv16741823RemappedPerfectNC_000012.11:g.123
010346_123010667de
l
GRCh37.p13First PassNC_000012.11Chr12123,010,346123,010,667

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)
nssv167418230.783
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