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nsv5410596

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 133 SVs from 37 studies. See in: genome view    
Submitted genomic112,556,141-112,556,192Question Mark
Overlapping variant regions from other studies: 133 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):113,477,297-113,477,348Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5410596Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4112,556,141112,556,192
nsv5410596RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4113,477,297113,477,348

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16955069alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16955069Submitted genomicNC_000004.12:g.112
556141_112556192in
s281
GRCh38 (hg38)NC_000004.12Chr4112,556,141112,556,192
nssv16955069RemappedPerfectNC_000004.11:g.113
477297_113477348in
s281
GRCh37.p13First PassNC_000004.11Chr4113,477,297113,477,348

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)
nssv169550690.002126398
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