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nsv5450594

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 27 studies. See in: genome view    
Submitted genomic219,159,535-219,159,589Question Mark
Overlapping variant regions from other studies: 136 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):220,024,257-220,024,311Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5450594Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2219,159,535219,159,589
nsv5450594RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2220,024,257220,024,311

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16925980deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16925980Submitted genomicNC_000002.12:g.219
159535_219159589de
l
GRCh38 (hg38)NC_000002.12Chr2219,159,535219,159,589
nssv16925980RemappedPerfectNC_000002.11:g.220
024257_220024311de
l
GRCh37.p13First PassNC_000002.11Chr2220,024,257220,024,311

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)
nssv16925980<0.00146402
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