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nsv5969964

  • 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: 98 SVs from 28 studies. See in: genome view    
Submitted genomic51,834,018-51,834,018Question Mark
Overlapping variant regions from other studies: 98 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):52,227,802-52,227,802Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5969964Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1251,834,01851,834,018
nsv5969964RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1252,227,80252,227,802

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17361780insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17361780Submitted genomicNC_000012.12:g.518
34018_51834019ins6
8
GRCh38 (hg38)NC_000012.12Chr1251,834,01851,834,018
nssv17361780RemappedPerfectNC_000012.11:g.522
27802_52227803ins6
8
GRCh37.p13First PassNC_000012.11Chr1252,227,80252,227,802

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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