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nsv5512183

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:308

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 43 studies. See in: genome view    
Submitted genomic94,275,572-94,275,879Question Mark
Overlapping variant regions from other studies: 115 SVs from 43 studies. See in: genome view    
Remapped(Score: Perfect):94,669,348-94,669,655Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5512183Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1294,275,57294,275,879
nsv5512183RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1294,669,34894,669,655

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684181deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684181Submitted genomicNC_000012.12:g.942
75572_94275879del
GRCh38 (hg38)NC_000012.12Chr1294,275,57294,275,879
nssv17684181RemappedPerfectNC_000012.11:g.946
69348_94669655del
GRCh37.p13First PassNC_000012.11Chr1294,669,34894,669,655

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)
nssv176841810.24715816404
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