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nsv5529141

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:505

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 117 SVs from 19 studies. See in: genome view    
Submitted genomic55,396,760-55,397,264Question Mark
Overlapping variant regions from other studies: 116 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):53,474,121-53,474,625Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5529141Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1755,396,76055,397,264
nsv5529141RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1753,474,12153,474,625

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724766deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724766Submitted genomicNC_000017.11:g.553
96760_55397264del
GRCh38 (hg38)NC_000017.11Chr1755,396,76055,397,264
nssv17724766RemappedPerfectNC_000017.10:g.534
74121_53474625del
GRCh37.p13First PassNC_000017.10Chr1753,474,12153,474,625

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)
nssv177247660.00186404
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