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nsv5449098

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:132

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 72 SVs from 18 studies. See in: genome view    
Submitted genomic15,643,948-15,644,079Question Mark
Overlapping variant regions from other studies: 72 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):15,685,455-15,685,586Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449098Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr315,643,94815,644,079
nsv5449098RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr315,685,45515,685,586

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16930964deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16930964Submitted genomicNC_000003.12:g.156
43948_15644079del
GRCh38 (hg38)NC_000003.12Chr315,643,94815,644,079
nssv16930964RemappedPerfectNC_000003.11:g.156
85455_15685586del
GRCh37.p13First PassNC_000003.11Chr315,685,45515,685,586

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)
nssv16930964<0.00116404
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