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nsv5397318

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:68

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 129 SVs from 25 studies. See in: genome view    
Submitted genomic53,935,467-53,935,534Question Mark
Overlapping variant regions from other studies: 129 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):54,401,140-54,401,207Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5397318Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr153,935,46753,935,534
nsv5397318RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr154,401,14054,401,207

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16905032alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16905032Submitted genomicNC_000001.11:g.539
35467_53935534ins2
78
GRCh38 (hg38)NC_000001.11Chr153,935,46753,935,534
nssv16905032RemappedPerfectNC_000001.10:g.544
01140_54401207ins2
78
GRCh37.p13First PassNC_000001.10Chr154,401,14054,401,207

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)
nssv169050320.006416376
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