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nsv5506097

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,150

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 122 SVs from 35 studies. See in: genome view    
Submitted genomic55,493,627-55,509,776Question Mark
Overlapping variant regions from other studies: 122 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):55,887,411-55,903,560Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5506097Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1255,493,62755,509,776
nsv5506097RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1255,887,41155,903,560

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17688520deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17688520Submitted genomicNC_000012.12:g.554
93627_55509776del
GRCh38 (hg38)NC_000012.12Chr1255,493,62755,509,776
nssv17688520RemappedPerfectNC_000012.11:g.558
87411_55903560del
GRCh37.p13First PassNC_000012.11Chr1255,887,41155,903,560

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)
nssv17688520<0.00126404
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