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nsv5509582

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,449

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 471 SVs from 68 studies. See in: genome view    
Submitted genomic8,208,854-8,238,302Question Mark
Overlapping variant regions from other studies: 471 SVs from 68 studies. See in: genome view    
Remapped(Score: Perfect):8,361,450-8,390,898Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5509582Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr128,208,8548,238,302
nsv5509582RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr128,361,4508,390,898

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17054767duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17054767Submitted genomicNC_000012.12:g.820
8854_8238302dup
GRCh38 (hg38)NC_000012.12Chr128,208,8548,238,302
nssv17054767RemappedPerfectNC_000012.11:g.836
1450_8390898dup
GRCh37.p13First PassNC_000012.11Chr128,361,4508,390,898

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)
nssv170547670.1278156404
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