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nsv5560415

  • 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: 155 SVs from 16 studies. See in: genome view    
Submitted genomic25,149,677-25,149,728Question Mark
Overlapping variant regions from other studies: 155 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):22,729,641-22,729,692Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5560415Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1825,149,67725,149,728
nsv5560415RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1822,729,64122,729,692

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17716728sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17716728Submitted genomicNC_000018.10:g.251
49677_25149728ins4
73
GRCh38 (hg38)NC_000018.10Chr1825,149,67725,149,728
nssv17716728RemappedPerfectNC_000018.9:g.2272
9641_22729692ins47
3
GRCh37.p13First PassNC_000018.9Chr1822,729,64122,729,692

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)
nssv17716728<0.00116404
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