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nsv5523186

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,132

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 147 SVs from 35 studies. See in: genome view    
Submitted genomic4,864,350-4,871,481Question Mark
Overlapping variant regions from other studies: 147 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):4,864,362-4,871,493Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523186Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr194,864,3504,871,481
nsv5523186RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr194,864,3624,871,493

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17720773deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17720773Submitted genomicNC_000019.10:g.486
4350_4871481del
GRCh38 (hg38)NC_000019.10Chr194,864,3504,871,481
nssv17720773RemappedPerfectNC_000019.9:g.4864
362_4871493del
GRCh37.p13First PassNC_000019.9Chr194,864,3624,871,493

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)
nssv17720773<0.00116404
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