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nsv5934426

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,955

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 203 SVs from 38 studies. See in: genome view    
Submitted genomic44,172,048-44,205,002Question Mark
Overlapping variant regions from other studies: 203 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):44,464,246-44,497,200Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5934426Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1544,172,04844,205,002
nsv5934426RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1544,464,24644,497,200

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17376070duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17376070Submitted genomicNC_000015.10:g.441
72048_44205002dup
GRCh38 (hg38)NC_000015.10Chr1544,172,04844,205,002
nssv17376070RemappedPerfectNC_000015.9:g.4446
4246_44497200dup
GRCh37.p13First PassNC_000015.9Chr1544,464,24644,497,200

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)
nssv173760700.00111582
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