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nsv5504133

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,293

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 29 studies. See in: genome view    
Submitted genomic42,895,837-42,897,129Question Mark
Overlapping variant regions from other studies: 136 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):43,188,035-43,189,327Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5504133Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1542,895,83742,897,129
nsv5504133RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1543,188,03543,189,327

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17701984deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17701984Submitted genomicNC_000015.10:g.428
95837_42897129del
GRCh38 (hg38)NC_000015.10Chr1542,895,83742,897,129
nssv17701984RemappedPerfectNC_000015.9:g.4318
8035_43189327del
GRCh37.p13First PassNC_000015.9Chr1543,188,03543,189,327

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)
nssv17701984<0.00116404
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