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nsv5153506

  • 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: 127 SVs from 21 studies. See in: genome view    
Submitted genomic55,393,970-55,393,985Question Mark
Overlapping variant regions from other studies: 126 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):53,471,331-53,471,346Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5153506Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1755,393,97055,393,985
nsv5153506RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1753,471,33153,471,346

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16716315alu insertionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16716315Submitted genomicNC_000017.11:g.553
93970_55393985ins2
72
GRCh38 (hg38)NC_000017.11Chr1755,393,97055,393,985
nssv16716315RemappedPerfectNC_000017.10:g.534
71331_53471346ins2
72
GRCh37.p13First PassNC_000017.10Chr1753,471,33153,471,346

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)
nssv167163150.5
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