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nsv5518970

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,155

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 26 studies. See in: genome view    
Submitted genomic10,448,867-10,451,021Question Mark
Overlapping variant regions from other studies: 99 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):10,542,724-10,544,878Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518970Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1610,448,86710,451,021
nsv5518970RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1610,542,72410,544,878

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704957deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704957Submitted genomicNC_000016.10:g.104
48867_10451021del
GRCh38 (hg38)NC_000016.10Chr1610,448,86710,451,021
nssv17704957RemappedPerfectNC_000016.9:g.1054
2724_10544878del
GRCh37.p13First PassNC_000016.9Chr1610,542,72410,544,878

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)
nssv17704957<0.00126404
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