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nsv5532827

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:258

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 109 SVs from 22 studies. See in: genome view    
Submitted genomic59,259,264-59,259,521Question Mark
Overlapping variant regions from other studies: 109 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):59,551,463-59,551,720Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5532827Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1559,259,26459,259,521
nsv5532827RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1559,551,46359,551,720

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17700950deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17700950Submitted genomicNC_000015.10:g.592
59264_59259521del
GRCh38 (hg38)NC_000015.10Chr1559,259,26459,259,521
nssv17700950RemappedPerfectNC_000015.9:g.5955
1463_59551720del
GRCh37.p13First PassNC_000015.9Chr1559,551,46359,551,720

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)
nssv17700950<0.00126404
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