nsv5563860

  • 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: 93 SVs from 20 studies. See in: genome view    
Submitted genomic19,897,691-19,897,742Question Mark
Overlapping variant regions from other studies: 93 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):19,878,335-19,878,386Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563860Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2019,897,69119,897,742
nsv5563860RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2019,878,33519,878,386

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17731438sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17731438Submitted genomicNC_000020.11:g.198
97691_19897742ins1
240
GRCh38 (hg38)NC_000020.11Chr2019,897,69119,897,742
nssv17731438RemappedPerfectNC_000020.10:g.198
78335_19878386ins1
240
GRCh37.p13First PassNC_000020.10Chr2019,878,33519,878,386

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)
nssv17731438<0.00126404
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