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nsv5490459

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:559

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 72 SVs from 15 studies. See in: genome view    
Submitted genomic31,473,988-31,474,546Question Mark
Overlapping variant regions from other studies: 72 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):31,762,917-31,763,475Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5490459Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1031,473,98831,474,546
nsv5490459RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1031,762,91731,763,475

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17031429deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17031429Submitted genomicNC_000010.11:g.314
73988_31474546del
GRCh38 (hg38)NC_000010.11Chr1031,473,98831,474,546
nssv17031429RemappedPerfectNC_000010.10:g.317
62917_31763475del
GRCh37.p13First PassNC_000010.10Chr1031,762,91731,763,475

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)
nssv17031429<0.00116404
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