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nsv5491998

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:393

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 126 SVs from 37 studies. See in: genome view    
Submitted genomic99,373,479-99,373,871Question Mark
Overlapping variant regions from other studies: 126 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):98,971,102-98,971,494Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5491998Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr799,373,47999,373,871
nsv5491998RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr798,971,10298,971,494

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17002890deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17002890Submitted genomicNC_000007.14:g.993
73479_99373871del
GRCh38 (hg38)NC_000007.14Chr799,373,47999,373,871
nssv17002890RemappedPerfectNC_000007.13:g.989
71102_98971494del
GRCh37.p13First PassNC_000007.13Chr798,971,10298,971,494

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)
nssv170028900.1479086180
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