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nsv5410701

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:46

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 15 studies. See in: genome view    
Submitted genomic102,778,257-102,778,302Question Mark
Overlapping variant regions from other studies: 94 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):102,648,988-102,649,033Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5410701Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11102,778,257102,778,302
nsv5410701RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11102,648,988102,649,033

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17049480alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17049480Submitted genomicNC_000011.10:g.102
778257_102778302in
s274
GRCh38 (hg38)NC_000011.10Chr11102,778,257102,778,302
nssv17049480RemappedPerfectNC_000011.9:g.1026
48988_102649033ins
274
GRCh37.p13First PassNC_000011.9Chr11102,648,988102,649,033

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)
nssv17049480<0.00126404
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