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nsv5891942

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
Submitted genomic10,214,590-10,214,640Question Mark
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):10,214,823-10,214,873Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5891942Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr610,214,59010,214,640
nsv5891942RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr610,214,82310,214,873

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17429273deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17429273Submitted genomicNC_000006.12:g.102
14590_10214640del
GRCh38 (hg38)NC_000006.12Chr610,214,59010,214,640
nssv17429273RemappedPerfectNC_000006.11:g.102
14823_10214873del
GRCh37.p13First PassNC_000006.11Chr610,214,82310,214,873

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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