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nsv5500345

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:87

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 112 SVs from 16 studies. See in: genome view    
Submitted genomic121,574,758-121,574,844Question Mark
Overlapping variant regions from other studies: 112 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):123,334,272-123,334,358Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5500345Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10121,574,758121,574,844
nsv5500345RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10123,334,272123,334,358

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17037857duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17037857Submitted genomicNC_000010.11:g.121
574758_121574844du
p
GRCh38 (hg38)NC_000010.11Chr10121,574,758121,574,844
nssv17037857RemappedPerfectNC_000010.10:g.123
334272_123334358du
p
GRCh37.p13First PassNC_000010.10Chr10123,334,272123,334,358

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)
nssv17037857<0.00126404
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