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nsv5401035

  • 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: 84 SVs from 17 studies. See in: genome view    
Submitted genomic95,845,135-95,845,186Question Mark
Overlapping variant regions from other studies: 84 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):97,604,892-97,604,943Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5401035Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1095,845,13595,845,186
nsv5401035RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1097,604,89297,604,943

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17038765alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17038765Submitted genomicNC_000010.11:g.958
45135_95845186ins2
79
GRCh38 (hg38)NC_000010.11Chr1095,845,13595,845,186
nssv17038765RemappedPerfectNC_000010.10:g.976
04892_97604943ins2
79
GRCh37.p13First PassNC_000010.10Chr1097,604,89297,604,943

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)
nssv17038765<0.00116404
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