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nsv5420444

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:290,125

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 879 SVs from 80 studies. See in: genome view    
Submitted genomic162,104,470-162,394,594Question Mark
Overlapping variant regions from other studies: 883 SVs from 80 studies. See in: genome view    
Remapped(Score: Perfect):162,074,260-162,364,384Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5420444Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1162,104,470162,394,594
nsv5420444RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1162,074,260162,364,384

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16891450duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16891450Submitted genomicNC_000001.11:g.162
104470_162394594du
p
GRCh38 (hg38)NC_000001.11Chr1162,104,470162,394,594
nssv16891450RemappedPerfectNC_000001.10:g.162
074260_162364384du
p
GRCh37.p13First PassNC_000001.10Chr1162,074,260162,364,384

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)
nssv16891450<0.00116404
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