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nsv5528871

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:62

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 37 studies. See in: genome view    
Submitted genomic15,623,517-15,623,578Question Mark
Overlapping variant regions from other studies: 124 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):15,734,327-15,734,388Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528871Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1915,623,51715,623,578
nsv5528871RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1915,734,32715,734,388

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721782deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721782Submitted genomicNC_000019.10:g.156
23517_15623578del
GRCh38 (hg38)NC_000019.10Chr1915,623,51715,623,578
nssv17721782RemappedPerfectNC_000019.9:g.1573
4327_15734388del
GRCh37.p13First PassNC_000019.9Chr1915,734,32715,734,388

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)
nssv177217820.1429016346
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