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nsv5405303

  • 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: 283 SVs from 38 studies. See in: genome view    
Submitted genomic10,275,094-10,275,145Question Mark
Overlapping variant regions from other studies: 283 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):10,132,604-10,132,655Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5405303Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr810,275,09410,275,145
nsv5405303RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr810,132,60410,132,655

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17007370alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17007370Submitted genomicNC_000008.11:g.102
75094_10275145ins2
81
GRCh38 (hg38)NC_000008.11Chr810,275,09410,275,145
nssv17007370RemappedPerfectNC_000008.10:g.101
32604_10132655ins2
81
GRCh37.p13First PassNC_000008.10Chr810,132,60410,132,655

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)
nssv170073700.021276404
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