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nsv5394666

  • 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: 128 SVs from 23 studies. See in: genome view    
Submitted genomic115,855,855-115,855,906Question Mark
Overlapping variant regions from other studies: 128 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):115,191,552-115,191,603Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5394666Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5115,855,855115,855,906
nsv5394666RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5115,191,552115,191,603

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16973718alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16973718Submitted genomicNC_000005.10:g.115
855855_115855906in
s276
GRCh38 (hg38)NC_000005.10Chr5115,855,855115,855,906
nssv16973718RemappedPerfectNC_000005.9:g.1151
91552_115191603ins
276
GRCh37.p13First PassNC_000005.9Chr5115,191,552115,191,603

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)
nssv16973718<0.00166404
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