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nsv5524303

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:380

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 149 SVs from 20 studies. See in: genome view    
Submitted genomic38,482,556-38,482,935Question Mark
Overlapping variant regions from other studies: 149 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):37,111,199-37,111,578Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5524303Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2038,482,55638,482,935
nsv5524303RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2037,111,19937,111,578

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732315deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732315Submitted genomicNC_000020.11:g.384
82556_38482935del
GRCh38 (hg38)NC_000020.11Chr2038,482,55638,482,935
nssv17732315RemappedPerfectNC_000020.10:g.371
11199_37111578del
GRCh37.p13First PassNC_000020.10Chr2037,111,19937,111,578

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)
nssv17732315<0.00116404
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