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nsv4283753

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:528,393

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 389 SVs from 20 studies. See in: genome view    
Remapped(Score: Good):59,995,939-60,524,331Question Mark
Overlapping variant regions from other studies: 386 SVs from 20 studies. See in: genome view    
Submitted genomic58,570,994-59,099,389Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4283753RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2059,995,93960,524,331
nsv4283753Submitted genomicGRCh37.p13Primary AssemblyNC_000020.10Chr2058,570,99459,099,389

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15862509deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15862509RemappedGoodNC_000020.11:g.599
95939_60524331del
GRCh38.p12First PassNC_000020.11Chr2059,995,93960,524,331
nssv15862509Submitted genomicNC_000020.10:g.585
70994_59099389del
GRCh37.p13NC_000020.10Chr2058,570,99459,099,389

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)
nssv158625094.6e-005121694
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