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nsv5561387

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75,642

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 267 SVs from 48 studies. See in: genome view    
Submitted genomic60,867,062-60,942,703Question Mark
Overlapping variant regions from other studies: 267 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):61,732,780-61,808,421Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5561387Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr460,867,06260,942,703
nsv5561387RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr461,732,78061,808,421

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16949128inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16949128Submitted genomicNC_000004.12:g.608
67062_60942703inv
GRCh38 (hg38)NC_000004.12Chr460,867,06260,942,703
nssv16949128RemappedPerfectNC_000004.11:g.617
32780_61808421inv
GRCh37.p13First PassNC_000004.11Chr461,732,78061,808,421

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)
nssv16949128<0.00136404
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