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nsv5552885

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 25 studies. See in: genome view    
Submitted genomic87,352,227-87,352,261Question Mark
Overlapping variant regions from other studies: 97 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):86,981,543-86,981,577Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5552885Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr787,352,22787,352,261
nsv5552885RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr786,981,54386,981,577

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16999023insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16999023Submitted genomicNC_000007.14:g.873
52227_87352261ins3
42
GRCh38 (hg38)NC_000007.14Chr787,352,22787,352,261
nssv16999023RemappedPerfectNC_000007.13:g.869
81543_86981577ins3
42
GRCh37.p13First PassNC_000007.13Chr786,981,54386,981,577

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)
nssv16999023<0.00116404
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