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nsv5457970

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,440

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 23 studies. See in: genome view    
Submitted genomic134,656,627-134,659,066Question Mark
Overlapping variant regions from other studies: 107 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):133,992,317-133,994,756Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5457970Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5134,656,627134,659,066
nsv5457970RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5133,992,317133,994,756

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16975058deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16975058Submitted genomicNC_000005.10:g.134
656627_134659066de
l
GRCh38 (hg38)NC_000005.10Chr5134,656,627134,659,066
nssv16975058RemappedPerfectNC_000005.9:g.1339
92317_133994756del
GRCh37.p13First PassNC_000005.9Chr5133,992,317133,994,756

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)
nssv16975058<0.00126404
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