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nsv5538536

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:176

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 101 SVs from 23 studies. See in: genome view    
Submitted genomic80,945,304-80,945,479Question Mark
Overlapping variant regions from other studies: 101 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):81,172,428-81,172,603Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5538536Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr280,945,30480,945,479
nsv5538536RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr281,172,42881,172,603

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16916296insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16916296Submitted genomicNC_000002.12:g.809
45304_80945479ins3
48
GRCh38 (hg38)NC_000002.12Chr280,945,30480,945,479
nssv16916296RemappedPerfectNC_000002.11:g.811
72428_81172603ins3
48
GRCh37.p13First PassNC_000002.11Chr281,172,42881,172,603

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)
nssv169162960.0513176266
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