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nsv5495074

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,060

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 110 SVs from 32 studies. See in: genome view    
Submitted genomic120,568,640-120,569,699Question Mark
Overlapping variant regions from other studies: 110 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):121,006,443-121,007,502Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5495074Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12120,568,640120,569,699
nsv5495074RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12121,006,443121,007,502

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684915deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684915Submitted genomicNC_000012.12:g.120
568640_120569699de
l
GRCh38 (hg38)NC_000012.12Chr12120,568,640120,569,699
nssv17684915RemappedPerfectNC_000012.11:g.121
006443_121007502de
l
GRCh37.p13First PassNC_000012.11Chr12121,006,443121,007,502

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)
nssv176849150.002126404
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