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nsv5425672

  • 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: 110 SVs from 21 studies. See in: genome view    
Submitted genomic45,058,875-45,058,926Question Mark
Overlapping variant regions from other studies: 110 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):43,687,516-43,687,567Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5425672Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2045,058,87545,058,926
nsv5425672RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2043,687,51643,687,567

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732594alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732594Submitted genomicNC_000020.11:g.450
58875_45058926ins2
77
GRCh38 (hg38)NC_000020.11Chr2045,058,87545,058,926
nssv17732594RemappedPerfectNC_000020.10:g.436
87516_43687567ins2
77
GRCh37.p13First PassNC_000020.10Chr2043,687,51643,687,567

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)
nssv17732594<0.00116404
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