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nsv5504920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,720

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 29 studies. See in: genome view    
Submitted genomic52,029,391-52,032,110Question Mark
Overlapping variant regions from other studies: 107 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):52,423,175-52,425,894Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5504920Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1252,029,39152,032,110
nsv5504920RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1252,423,17552,425,894

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058738deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058738Submitted genomicNC_000012.12:g.520
29391_52032110del
GRCh38 (hg38)NC_000012.12Chr1252,029,39152,032,110
nssv17058738RemappedPerfectNC_000012.11:g.524
23175_52425894del
GRCh37.p13First PassNC_000012.11Chr1252,423,17552,425,894

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)
nssv17058738<0.00116404
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