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nsv5454427

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:885

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 83 SVs from 23 studies. See in: genome view    
Submitted genomic39,262,225-39,263,109Question Mark
Overlapping variant regions from other studies: 83 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):39,262,327-39,263,211Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5454427Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr539,262,22539,263,109
nsv5454427RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr539,262,32739,263,211

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16964856duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16964856Submitted genomicNC_000005.10:g.392
62225_39263109dup
GRCh38 (hg38)NC_000005.10Chr539,262,22539,263,109
nssv16964856RemappedPerfectNC_000005.9:g.3926
2327_39263211dup
GRCh37.p13First PassNC_000005.9Chr539,262,32739,263,211

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)
nssv16964856<0.00156404
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