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nsv5497289

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:734

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 31 studies. See in: genome view    
Submitted genomic94,165,580-94,166,313Question Mark
Overlapping variant regions from other studies: 98 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):94,559,356-94,560,089Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5497289Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1294,165,58094,166,313
nsv5497289RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1294,559,35694,560,089

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684174deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684174Submitted genomicNC_000012.12:g.941
65580_94166313del
GRCh38 (hg38)NC_000012.12Chr1294,165,58094,166,313
nssv17684174RemappedPerfectNC_000012.11:g.945
59356_94560089del
GRCh37.p13First PassNC_000012.11Chr1294,559,35694,560,089

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)
nssv176841740.005336404
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