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nsv4265791

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:205

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 18 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):40,693,251-40,693,455Question Mark
Overlapping variant regions from other studies: 16 SVs from 6 studies. See in: genome view    
Submitted genomic38,849,503-38,849,707Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4265791RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1740,693,25140,693,455
nsv4265791Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1738,849,50338,849,707

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15834384deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15834384RemappedPerfectNC_000017.11:g.406
93251_40693455del
GRCh38.p12First PassNC_000017.11Chr1740,693,25140,693,455
nssv15834384Submitted genomicNC_000017.10:g.388
49503_38849707del
GRCh37.p13NC_000017.10Chr1738,849,50338,849,707

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)
nssv158343844.6e-005121694
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