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nsv5547577

  • 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: 129 SVs from 30 studies. See in: genome view    
Submitted genomic73,211,082-73,211,133Question Mark
Overlapping variant regions from other studies: 129 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):74,076,799-74,076,850Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5547577Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr473,211,08273,211,133
nsv5547577RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr474,076,79974,076,850

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16952232insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16952232Submitted genomicNC_000004.12:g.732
11082_73211133ins1
62
GRCh38 (hg38)NC_000004.12Chr473,211,08273,211,133
nssv16952232RemappedPerfectNC_000004.11:g.740
76799_74076850ins1
62
GRCh37.p13First PassNC_000004.11Chr474,076,79974,076,850

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)
nssv16952232<0.00126404
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