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nsv4509209

  • 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: 24 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):28,727,082-28,727,082Question Mark
Overlapping variant regions from other studies: 24 SVs from 6 studies. See in: genome view    
Submitted genomic27,054,100-27,054,100Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4509209RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1728,727,08228,727,082
nsv4509209Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1727,054,10027,054,100

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16016265alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16016265RemappedPerfectNC_000017.11:g.287
27082_28727083ins1
43
GRCh38.p12First PassNC_000017.11Chr1728,727,08228,727,082
nssv16016265Submitted genomicNC_000017.10:g.270
54100_27054101ins1
43
GRCh37.p13NC_000017.10Chr1727,054,10027,054,100

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)
nssv160162654.6e-005121694
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