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nsv5146737

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 22 studies. See in: genome view    
Submitted genomic75,123,911-75,123,928Question Mark
Overlapping variant regions from other studies: 136 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):73,120,006-73,120,023Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5146737Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,123,91175,123,928
nsv5146737RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,120,00673,120,023

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16722993alu insertionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16722993Submitted genomicNC_000017.11:g.751
23911_75123928ins3
52
GRCh38 (hg38)NC_000017.11Chr1775,123,91175,123,928
nssv16722993RemappedPerfectNC_000017.10:g.731
20006_73120023ins3
52
GRCh37.p13First PassNC_000017.10Chr1773,120,00673,120,023

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)
nssv167229930.636
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