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nsv5953006

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 306 SVs from 42 studies. See in: genome view    
Submitted genomic15,041,744-15,041,744Question Mark
Overlapping variant regions from other studies: 306 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):14,899,253-14,899,253Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5953006Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr815,041,74415,041,744
nsv5953006RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr814,899,25314,899,253

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17435983insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17435983Submitted genomicNC_000008.11:g.150
41744_15041745ins1
60
GRCh38 (hg38)NC_000008.11Chr815,041,74415,041,744
nssv17435983RemappedPerfectNC_000008.10:g.148
99253_14899254ins1
60
GRCh37.p13First PassNC_000008.10Chr814,899,25314,899,253

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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