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nsv5515557

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:345,936

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 877 SVs from 67 studies. See in: genome view    
Submitted genomic51,768,552-52,114,487Question Mark
Overlapping variant regions from other studies: 877 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):52,271,805-52,617,740Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5515557Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1951,768,55252,114,487
nsv5515557RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1952,271,80552,617,740

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724134duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724134Submitted genomicNC_000019.10:g.517
68552_52114487dup
GRCh38 (hg38)NC_000019.10Chr1951,768,55252,114,487
nssv17724134RemappedPerfectNC_000019.9:g.5227
1805_52617740dup
GRCh37.p13First PassNC_000019.9Chr1952,271,80552,617,740

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)
nssv17724134<0.00126404
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