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nsv5410402

  • 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: 152 SVs from 24 studies. See in: genome view    
Submitted genomic38,052,197-38,052,248Question Mark
Overlapping variant regions from other studies: 152 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):38,279,340-38,279,391Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5410402Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr238,052,19738,052,248
nsv5410402RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr238,279,34038,279,391

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16911853alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16911853Submitted genomicNC_000002.12:g.380
52197_38052248ins2
25
GRCh38 (hg38)NC_000002.12Chr238,052,19738,052,248
nssv16911853RemappedPerfectNC_000002.11:g.382
79340_38279391ins2
25
GRCh37.p13First PassNC_000002.11Chr238,279,34038,279,391

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)
nssv16911853<0.00136404
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