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nsv4644870

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:376

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 172 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):5,553,900-5,554,275Question Mark
Overlapping variant regions from other studies: 172 SVs from 48 studies. See in: genome view    
Submitted genomic5,534,546-5,534,921Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4644870RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr205,553,9005,554,275
nsv4644870Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000020.10Chr205,534,5465,534,921

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16197829alu deletionCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16197829RemappedPerfectNC_000020.11:g.555
3900_5554275del
GRCh38.p12First PassNC_000020.11Chr205,553,9005,554,275
nssv16197829Submitted genomicNC_000020.10:g.553
4546_5534921del
GRCh37 (hg19)NC_000020.10Chr205,534,5465,534,921

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)
nssv161978290.2814025008
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