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nsv5505357

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,438

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 89 SVs from 36 studies. See in: genome view    
Submitted genomic18,884,283-18,886,720Question Mark
Overlapping variant regions from other studies: 89 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):18,905,830-18,908,267Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5505357Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1118,884,28318,886,720
nsv5505357RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1118,905,83018,908,267

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17044688deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17044688Submitted genomicNC_000011.10:g.188
84283_18886720del
GRCh38 (hg38)NC_000011.10Chr1118,884,28318,886,720
nssv17044688RemappedPerfectNC_000011.9:g.1890
5830_18908267del
GRCh37.p13First PassNC_000011.9Chr1118,905,83018,908,267

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)
nssv17044688<0.00136404
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