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nsv5524295

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:112

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 186 SVs from 30 studies. See in: genome view    
Submitted genomic82,274,146-82,274,257Question Mark
Overlapping variant regions from other studies: 186 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):80,232,022-80,232,133Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5524295Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1782,274,14682,274,257
nsv5524295RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1780,232,02280,232,133

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17715665duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17715665Submitted genomicNC_000017.11:g.822
74146_82274257dup
GRCh38 (hg38)NC_000017.11Chr1782,274,14682,274,257
nssv17715665RemappedPerfectNC_000017.10:g.802
32022_80232133dup
GRCh37.p13First PassNC_000017.10Chr1780,232,02280,232,133

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)
nssv17715665<0.00116404
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