U.S. flag

An official website of the United States government

nsv5558422

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,445

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 25 studies. See in: genome view    
Submitted genomic135,946,807-135,957,251Question Mark
Overlapping variant regions from other studies: 94 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):135,282,496-135,292,940Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5558422Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5135,946,807135,957,251
nsv5558422RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5135,282,496135,292,940

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16974400sequence alterationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16974400Submitted genomicGRCh38 (hg38)NC_000005.10Chr5135,946,807135,957,251
nssv16974400RemappedPerfectGRCh37.p13First PassNC_000005.9Chr5135,282,496135,292,940

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)
nssv16974400<0.00126404
You are here: NCBI
Support Center