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nsv5528327

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,659

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 33 studies. See in: genome view    
Submitted genomic55,793,065-55,795,723Question Mark
Overlapping variant regions from other studies: 136 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):56,304,431-56,307,089Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528327Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1955,793,06555,795,723
nsv5528327RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1956,304,43156,307,089

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17725715deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17725715Submitted genomicNC_000019.10:g.557
93065_55795723del
GRCh38 (hg38)NC_000019.10Chr1955,793,06555,795,723
nssv17725715RemappedPerfectNC_000019.9:g.5630
4431_56307089del
GRCh37.p13First PassNC_000019.9Chr1956,304,43156,307,089

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)
nssv17725715<0.00116404
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