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nsv5939238

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:90,505

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 366 SVs from 51 studies. See in: genome view    
Submitted genomic50,255,984-50,346,488Question Mark
Overlapping variant regions from other studies: 366 SVs from 51 studies. See in: genome view    
Remapped(Score: Perfect):50,649,767-50,740,271Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5939238Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1250,255,98450,346,488
nsv5939238RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1250,649,76750,740,271

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17365804duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17365804Submitted genomicNC_000012.12:g.502
55984_50346488dup
GRCh38 (hg38)NC_000012.12Chr1250,255,98450,346,488
nssv17365804RemappedPerfectNC_000012.11:g.506
49767_50740271dup
GRCh37.p13First PassNC_000012.11Chr1250,649,76750,740,271

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)
nssv173658040.00111780
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