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nsv5505145

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:195

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 85 SVs from 23 studies. See in: genome view    
Submitted genomic94,217,156-94,217,350Question Mark
Overlapping variant regions from other studies: 85 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):94,610,932-94,611,126Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5505145Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1294,217,15694,217,350
nsv5505145RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1294,610,93294,611,126

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684178deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684178Submitted genomicNC_000012.12:g.942
17156_94217350del
GRCh38 (hg38)NC_000012.12Chr1294,217,15694,217,350
nssv17684178RemappedPerfectNC_000012.11:g.946
10932_94611126del
GRCh37.p13First PassNC_000012.11Chr1294,610,93294,611,126

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)
nssv17684178<0.00116404
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