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nsv5518045

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,953

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 29 studies. See in: genome view    
Submitted genomic57,639,616-57,643,568Question Mark
Overlapping variant regions from other studies: 124 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):58,150,984-58,154,936Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518045Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1957,639,61657,643,568
nsv5518045RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1958,150,98458,154,936

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724358deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724358Submitted genomicNC_000019.10:g.576
39616_57643568del
GRCh38 (hg38)NC_000019.10Chr1957,639,61657,643,568
nssv17724358RemappedPerfectNC_000019.9:g.5815
0984_58154936del
GRCh37.p13First PassNC_000019.9Chr1958,150,98458,154,936

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)
nssv17724358<0.00116404
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