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nsv4512627

  • 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: 25 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):59,516,373-59,516,373Question Mark
Overlapping variant regions from other studies: 25 SVs from 5 studies. See in: genome view    
Submitted genomic59,983,091-59,983,091Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4512627RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1459,516,37359,516,373
nsv4512627Submitted genomicGRCh37.p13Primary AssemblyNC_000014.8Chr1459,983,09159,983,091

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16009739alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16009739RemappedPerfectNC_000014.9:g.5951
6373_59516374ins28
0
GRCh38.p12First PassNC_000014.9Chr1459,516,37359,516,373
nssv16009739Submitted genomicNC_000014.8:g.5998
3091_59983092ins28
0
GRCh37.p13NC_000014.8Chr1459,983,09159,983,091

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)
nssv16009739<0.001321694
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