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nsv5412937

  • 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: 90 SVs from 19 studies. See in: genome view    
Submitted genomic52,518,048-52,518,099Question Mark
Overlapping variant regions from other studies: 90 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):52,382,846-52,382,897Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5412937Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr652,518,04852,518,099
nsv5412937RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr652,382,84652,382,897

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16982803alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16982803Submitted genomicNC_000006.12:g.525
18048_52518099ins2
81
GRCh38 (hg38)NC_000006.12Chr652,518,04852,518,099
nssv16982803RemappedPerfectNC_000006.11:g.523
82846_52382897ins2
81
GRCh37.p13First PassNC_000006.11Chr652,382,84652,382,897

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)
nssv16982803<0.00116404
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