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nsv5503970

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:77

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 84 SVs from 24 studies. See in: genome view    
Submitted genomic109,760,026-109,760,102Question Mark
Overlapping variant regions from other studies: 84 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):110,197,831-110,197,907Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5503970Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12109,760,026109,760,102
nsv5503970RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12110,197,831110,197,907

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684387duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684387Submitted genomicNC_000012.12:g.109
760026_109760102du
p
GRCh38 (hg38)NC_000012.12Chr12109,760,026109,760,102
nssv17684387RemappedPerfectNC_000012.11:g.110
197831_110197907du
p
GRCh37.p13First PassNC_000012.11Chr12110,197,831110,197,907

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)
nssv17684387<0.00136404
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