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nsv5555012

  • 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: 91 SVs from 22 studies. See in: genome view    
Submitted genomic45,112,998-45,113,049Question Mark
Overlapping variant regions from other studies: 91 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):45,154,490-45,154,541Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5555012Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr345,112,99845,113,049
nsv5555012RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr345,154,49045,154,541

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933691line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933691Submitted genomicNC_000003.12:g.451
12998_45113049ins6
017
GRCh38 (hg38)NC_000003.12Chr345,112,99845,113,049
nssv16933691RemappedPerfectNC_000003.11:g.451
54490_45154541ins6
017
GRCh37.p13First PassNC_000003.11Chr345,154,49045,154,541

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)
nssv16933691<0.00116404
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