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nsv5470354

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:953

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 22 studies. See in: genome view    
Submitted genomic149,619,752-149,620,704Question Mark
Overlapping variant regions from other studies: 96 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):148,999,315-149,000,267Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5470354Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5149,619,752149,620,704
nsv5470354RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5148,999,315149,000,267

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16975642deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16975642Submitted genomicNC_000005.10:g.149
619752_149620704de
l
GRCh38 (hg38)NC_000005.10Chr5149,619,752149,620,704
nssv16975642RemappedPerfectNC_000005.9:g.1489
99315_149000267del
GRCh37.p13First PassNC_000005.9Chr5148,999,315149,000,267

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)
nssv16975642<0.00116404
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