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nsv5528019

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,679

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 229 SVs from 53 studies. See in: genome view    
Submitted genomic43,643,259-43,645,937Question Mark
Overlapping variant regions from other studies: 229 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):42,271,899-42,274,577Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528019Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2043,643,25943,645,937
nsv5528019RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2042,271,89942,274,577

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17726008deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17726008Submitted genomicNC_000020.11:g.436
43259_43645937del
GRCh38 (hg38)NC_000020.11Chr2043,643,25943,645,937
nssv17726008RemappedPerfectNC_000020.10:g.422
71899_42274577del
GRCh37.p13First PassNC_000020.10Chr2042,271,89942,274,577

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv177260080.61539396404
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