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nsv5404116

  • 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: 122 SVs from 27 studies. See in: genome view    
Submitted genomic65,498,232-65,498,283Question Mark
Overlapping variant regions from other studies: 122 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):65,265,703-65,265,754Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5404116Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1165,498,23265,498,283
nsv5404116RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1165,265,70365,265,754

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17046753alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17046753Submitted genomicNC_000011.10:g.654
98232_65498283ins2
81
GRCh38 (hg38)NC_000011.10Chr1165,498,23265,498,283
nssv17046753RemappedPerfectNC_000011.9:g.6526
5703_65265754ins28
1
GRCh37.p13First PassNC_000011.9Chr1165,265,70365,265,754

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)
nssv17046753<0.00126404
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