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nsv5518576

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:750

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
Submitted genomic3,124,460-3,125,209Question Mark
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):3,105,106-3,105,855Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518576Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr203,124,4603,125,209
nsv5518576RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr203,105,1063,105,855

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17730386deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17730386Submitted genomicNC_000020.11:g.312
4460_3125209del
GRCh38 (hg38)NC_000020.11Chr203,124,4603,125,209
nssv17730386RemappedPerfectNC_000020.10:g.310
5106_3105855del
GRCh37.p13First PassNC_000020.10Chr203,105,1063,105,855

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)
nssv177303860.003176400
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