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nsv5549040

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 18 studies. See in: genome view    
Submitted genomic45,038,803-45,038,818Question Mark
Overlapping variant regions from other studies: 105 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):43,667,444-43,667,459Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5549040Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2045,038,80345,038,818
nsv5549040RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2043,667,44443,667,459

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732591insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732591Submitted genomicNC_000020.11:g.450
38803_45038818ins8
6
GRCh38 (hg38)NC_000020.11Chr2045,038,80345,038,818
nssv17732591RemappedPerfectNC_000020.10:g.436
67444_43667459ins8
6
GRCh37.p13First PassNC_000020.10Chr2043,667,44443,667,459

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)
nssv17732591<0.00126404
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