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nsv5933764

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,822

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 200 SVs from 32 studies. See in: genome view    
Submitted genomic83,782,235-83,791,056Question Mark
Overlapping variant regions from other studies: 201 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):84,450,987-84,459,808Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5933764Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1583,782,23583,791,056
nsv5933764RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1584,450,98784,459,808

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17384437duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17384437Submitted genomicNC_000015.10:g.837
82235_83791056dup
GRCh38 (hg38)NC_000015.10Chr1583,782,23583,791,056
nssv17384437RemappedPerfectNC_000015.9:g.8445
0987_84459808dup
GRCh37.p13First PassNC_000015.9Chr1584,450,98784,459,808

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)
nssv173844370.00111820
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