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nsv5395029

  • 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: 125 SVs from 22 studies. See in: genome view    
Submitted genomic53,935,553-53,935,604Question Mark
Overlapping variant regions from other studies: 125 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):54,401,226-54,401,277Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5395029Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr153,935,55353,935,604
nsv5395029RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr154,401,22654,401,277

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16905034alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16905034Submitted genomicNC_000001.11:g.539
35553_53935604ins2
77
GRCh38 (hg38)NC_000001.11Chr153,935,55353,935,604
nssv16905034RemappedPerfectNC_000001.10:g.544
01226_54401277ins2
77
GRCh37.p13First PassNC_000001.10Chr154,401,22654,401,277

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)
nssv169050340.004276384
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