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nsv5411966

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 240 SVs from 32 studies. See in: genome view    
Submitted genomic181,865,470-181,865,543Question Mark
Overlapping variant regions from other studies: 240 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):182,786,623-182,786,696Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5411966Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4181,865,470181,865,543
nsv5411966RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4182,786,623182,786,696

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16961163alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16961163Submitted genomicNC_000004.12:g.181
865470_181865543in
s280
GRCh38 (hg38)NC_000004.12Chr4181,865,470181,865,543
nssv16961163RemappedPerfectNC_000004.11:g.182
786623_182786696in
s280
GRCh37.p13First PassNC_000004.11Chr4182,786,623182,786,696

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)
nssv16961163<0.00146404
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