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nsv5414350

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:115

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 20 studies. See in: genome view    
Submitted genomic56,693,156-56,693,270Question Mark
Overlapping variant regions from other studies: 119 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):57,158,829-57,158,943Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5414350Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr156,693,15656,693,270
nsv5414350RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr157,158,82957,158,943

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16903043deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16903043Submitted genomicNC_000001.11:g.566
93156_56693270del
GRCh38 (hg38)NC_000001.11Chr156,693,15656,693,270
nssv16903043RemappedPerfectNC_000001.10:g.571
58829_57158943del
GRCh37.p13First PassNC_000001.10Chr157,158,82957,158,943

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)
nssv16903043<0.00126404
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