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nsv5442332

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,013

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 101 SVs from 26 studies. See in: genome view    
Submitted genomic52,690,553-52,692,565Question Mark
Overlapping variant regions from other studies: 101 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):52,724,569-52,726,581Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5442332Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr352,690,55352,692,565
nsv5442332RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr352,724,56952,726,581

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16932773deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16932773Submitted genomicNC_000003.12:g.526
90553_52692565del
GRCh38 (hg38)NC_000003.12Chr352,690,55352,692,565
nssv16932773RemappedPerfectNC_000003.11:g.527
24569_52726581del
GRCh37.p13First PassNC_000003.11Chr352,724,56952,726,581

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)
nssv16932773<0.00116404
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