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nsv5559154

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 135 SVs from 27 studies. See in: genome view    
Submitted genomic14,374,988-14,374,993Question Mark
Overlapping variant regions from other studies: 136 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):14,527,922-14,527,927Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5559154Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1214,374,98814,374,993
nsv5559154RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1214,527,92214,527,927

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17056012sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17056012Submitted genomicNC_000012.12:g.143
74988_14374993ins7
41
GRCh38 (hg38)NC_000012.12Chr1214,374,98814,374,993
nssv17056012RemappedPerfectNC_000012.11:g.145
27922_14527927ins7
41
GRCh37.p13First PassNC_000012.11Chr1214,527,92214,527,927

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)
nssv170560120.00196404
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