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nsv5466197

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57,324

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 291 SVs from 37 studies. See in: genome view    
Submitted genomic112,130,729-112,188,052Question Mark
Overlapping variant regions from other studies: 291 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):111,466,426-111,523,749Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5466197Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5112,130,729112,188,052
nsv5466197RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5111,466,426111,523,749

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16971928duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16971928Submitted genomicNC_000005.10:g.112
130729_112188052du
p
GRCh38 (hg38)NC_000005.10Chr5112,130,729112,188,052
nssv16971928RemappedPerfectNC_000005.9:g.1114
66426_111523749dup
GRCh37.p13First PassNC_000005.9Chr5111,466,426111,523,749

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)
nssv16971928<0.00126404
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