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nsv6293466

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):5,821,374-5,821,425Question Mark
Overlapping variant regions from other studies: 91 SVs from 32 studies. See in: genome view    
Submitted genomic5,842,604-5,842,655Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6293466RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr115,821,3745,821,425
nsv6293466Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr115,842,6045,842,655

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17677188alu insertionCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17677188RemappedPerfectNC_000011.10:g.582
1374_5821425ins?
GRCh38.p12First PassNC_000011.10Chr115,821,3745,821,425
nssv17677188Submitted genomicNC_000011.9:g.5842
604_5842655ins?
GRCh37 (hg19)NC_000011.9Chr115,842,6045,842,655

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv176771880.0342216404
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