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nsv5489807

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,251

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 78 SVs from 19 studies. See in: genome view    
Submitted genomic42,050,897-42,053,147Question Mark
Overlapping variant regions from other studies: 78 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):42,090,496-42,092,746Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489807Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr742,050,89742,053,147
nsv5489807RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr742,090,49642,092,746

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16995215deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16995215Submitted genomicNC_000007.14:g.420
50897_42053147del
GRCh38 (hg38)NC_000007.14Chr742,050,89742,053,147
nssv16995215RemappedPerfectNC_000007.13:g.420
90496_42092746del
GRCh37.p13First PassNC_000007.13Chr742,090,49642,092,746

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)
nssv16995215<0.00136404
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