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nsv5396681

  • 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: 117 SVs from 26 studies. See in: genome view    
Submitted genomic70,728,032-70,728,083Question Mark
Overlapping variant regions from other studies: 117 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):71,593,749-71,593,800Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5396681Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr470,728,03270,728,083
nsv5396681RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr471,593,74971,593,800

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16950643alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16950643Submitted genomicNC_000004.12:g.707
28032_70728083ins2
80
GRCh38 (hg38)NC_000004.12Chr470,728,03270,728,083
nssv16950643RemappedPerfectNC_000004.11:g.715
93749_71593800ins2
80
GRCh37.p13First PassNC_000004.11Chr471,593,74971,593,800

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)
nssv16950643<0.00126404
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