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nsv5555062

  • 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: 84 SVs from 25 studies. See in: genome view    
Submitted genomic79,466,925-79,466,976Question Mark
Overlapping variant regions from other studies: 84 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):79,096,241-79,096,292Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5555062Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr779,466,92579,466,976
nsv5555062RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr779,096,24179,096,292

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16998853sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16998853Submitted genomicNC_000007.14:g.794
66925_79466976ins1
240
GRCh38 (hg38)NC_000007.14Chr779,466,92579,466,976
nssv16998853RemappedPerfectNC_000007.13:g.790
96241_79096292ins1
240
GRCh37.p13First PassNC_000007.13Chr779,096,24179,096,292

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)
nssv16998853<0.00126404
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