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nsv5510107

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 100 SVs from 19 studies. See in: genome view    
Submitted genomic102,588,795-102,588,873Question Mark
Overlapping variant regions from other studies: 100 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):102,459,526-102,459,604Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5510107Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11102,588,795102,588,873
nsv5510107RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11102,459,526102,459,604

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17049462deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17049462Submitted genomicNC_000011.10:g.102
588795_102588873de
l
GRCh38 (hg38)NC_000011.10Chr11102,588,795102,588,873
nssv17049462RemappedPerfectNC_000011.9:g.1024
59526_102459604del
GRCh37.p13First PassNC_000011.9Chr11102,459,526102,459,604

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)
nssv17049462<0.00116404
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