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nsv5467357

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,292

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 26 studies. See in: genome view    
Submitted genomic131,279,631-131,281,922Question Mark
Overlapping variant regions from other studies: 114 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):130,615,324-130,617,615Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5467357Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5131,279,631131,281,922
nsv5467357RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5130,615,324130,617,615

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16973532duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16973532Submitted genomicNC_000005.10:g.131
279631_131281922du
p
GRCh38 (hg38)NC_000005.10Chr5131,279,631131,281,922
nssv16973532RemappedPerfectNC_000005.9:g.1306
15324_130617615dup
GRCh37.p13First PassNC_000005.9Chr5130,615,324130,617,615

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)
nssv16973532<0.00126404
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