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nsv5517445

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,956

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 228 SVs from 37 studies. See in: genome view    
Submitted genomic43,862,438-43,888,393Question Mark
Overlapping variant regions from other studies: 226 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):41,939,806-41,965,761Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5517445Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1743,862,43843,888,393
nsv5517445RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1741,939,80641,965,761

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713263duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713263Submitted genomicNC_000017.11:g.438
62438_43888393dup
GRCh38 (hg38)NC_000017.11Chr1743,862,43843,888,393
nssv17713263RemappedPerfectNC_000017.10:g.419
39806_41965761dup
GRCh37.p13First PassNC_000017.10Chr1741,939,80641,965,761

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)
nssv17713263<0.00116404
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