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nsv4568427

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 30 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):54,538,591-54,538,591Question Mark
Overlapping variant regions from other studies: 30 SVs from 6 studies. See in: genome view    
Submitted genomic53,834,421-53,834,421Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4568427RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr554,538,59154,538,591
nsv4568427Submitted genomicGRCh37.p13Primary AssemblyNC_000005.9Chr553,834,42153,834,421

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16061961sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16061961RemappedPerfectNC_000005.10:g.545
38591_54538592ins1
140
GRCh38.p12First PassNC_000005.10Chr554,538,59154,538,591
nssv16061961Submitted genomicNC_000005.9:g.5383
4421_53834422ins11
40
GRCh37.p13NC_000005.9Chr553,834,42153,834,421

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)
nssv16061961<0.001321692
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