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nsv5445664

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,536

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 93 SVs from 20 studies. See in: genome view    
Submitted genomic231,080,941-231,082,476Question Mark
Overlapping variant regions from other studies: 93 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):231,945,655-231,947,190Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5445664Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2231,080,941231,082,476
nsv5445664RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2231,945,655231,947,190

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928547duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928547Submitted genomicNC_000002.12:g.231
080941_231082476du
p
GRCh38 (hg38)NC_000002.12Chr2231,080,941231,082,476
nssv16928547RemappedPerfectNC_000002.11:g.231
945655_231947190du
p
GRCh37.p13First PassNC_000002.11Chr2231,945,655231,947,190

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)
nssv16928547<0.00166404
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