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nsv5514578

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,120

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 75 SVs from 24 studies. See in: genome view    
Submitted genomic57,293,973-57,299,092Question Mark
Overlapping variant regions from other studies: 75 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):57,805,341-57,810,460Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514578Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1957,293,97357,299,092
nsv5514578RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1957,805,34157,810,460

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724331deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724331Submitted genomicNC_000019.10:g.572
93973_57299092del
GRCh38 (hg38)NC_000019.10Chr1957,293,97357,299,092
nssv17724331RemappedPerfectNC_000019.9:g.5780
5341_57810460del
GRCh37.p13First PassNC_000019.9Chr1957,805,34157,810,460

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)
nssv17724331<0.00116404
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