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nsv5973717

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:390,009

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 981 SVs from 69 studies. See in: genome view    
Submitted genomic68,441,270-68,831,278Question Mark
Overlapping variant regions from other studies: 981 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):68,907,987-69,297,995Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5973717Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1468,441,27068,831,278
nsv5973717RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1468,907,98769,297,995

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17385425inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17385425Submitted genomicNC_000014.9:g.6844
1270_68831278inv
GRCh38 (hg38)NC_000014.9Chr1468,441,27068,831,278
nssv17385425RemappedPerfectNC_000014.8:g.6890
7987_69297995inv
GRCh37.p13First PassNC_000014.8Chr1468,907,98769,297,995

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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