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nsv5405347

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 236 SVs from 27 studies. See in: genome view    
Submitted genomic181,265,286-181,265,310Question Mark
Overlapping variant regions from other studies: 236 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):182,186,439-182,186,463Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5405347Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4181,265,286181,265,310
nsv5405347RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4182,186,439182,186,463

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16961151alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16961151Submitted genomicNC_000004.12:g.181
265286_181265310in
s280
GRCh38 (hg38)NC_000004.12Chr4181,265,286181,265,310
nssv16961151RemappedPerfectNC_000004.11:g.182
186439_182186463in
s280
GRCh37.p13First PassNC_000004.11Chr4182,186,439182,186,463

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)
nssv16961151<0.00146404
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