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nsv5407688

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 144 SVs from 24 studies. See in: genome view    
Submitted genomic78,645,278-78,645,329Question Mark
Overlapping variant regions from other studies: 144 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):79,110,963-79,111,014Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5407688Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr178,645,27878,645,329
nsv5407688RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr179,110,96379,111,014

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16907452alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16907452Submitted genomicNC_000001.11:g.786
45278_78645329ins2
81
GRCh38 (hg38)NC_000001.11Chr178,645,27878,645,329
nssv16907452RemappedPerfectNC_000001.10:g.791
10963_79111014ins2
81
GRCh37.p13First PassNC_000001.10Chr179,110,96379,111,014

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)
nssv16907452<0.00126404
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