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nsv5523858

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,572

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 33 studies. See in: genome view    
Submitted genomic27,554,273-27,559,844Question Mark
Overlapping variant regions from other studies: 132 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):27,565,594-27,571,165Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523858Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1627,554,27327,559,844
nsv5523858RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1627,565,59427,571,165

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17706279deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17706279Submitted genomicNC_000016.10:g.275
54273_27559844del
GRCh38 (hg38)NC_000016.10Chr1627,554,27327,559,844
nssv17706279RemappedPerfectNC_000016.9:g.2756
5594_27571165del
GRCh37.p13First PassNC_000016.9Chr1627,565,59427,571,165

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)
nssv17706279<0.00116404
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