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nsv5087840

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 28 studies. See in: genome view    
Submitted genomic115,855,844-115,855,855Question Mark
Overlapping variant regions from other studies: 153 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):115,191,541-115,191,552Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5087840Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5115,855,844115,855,855
nsv5087840RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5115,191,541115,191,552

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16642600alu insertionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16642600Submitted genomicNC_000005.10:g.115
855844_115855855in
s161
GRCh38 (hg38)NC_000005.10Chr5115,855,844115,855,855
nssv16642600RemappedPerfectNC_000005.9:g.1151
91541_115191552ins
161
GRCh37.p13First PassNC_000005.9Chr5115,191,541115,191,552

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)
nssv166426000.524
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