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nsv5506924

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:516

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 92 SVs from 26 studies. See in: genome view    
Submitted genomic104,124,525-104,125,040Question Mark
Overlapping variant regions from other studies: 92 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):104,518,303-104,518,818Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5506924Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12104,124,525104,125,040
nsv5506924RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12104,518,303104,518,818

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17690502deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17690502Submitted genomicNC_000012.12:g.104
124525_104125040de
l
GRCh38 (hg38)NC_000012.12Chr12104,124,525104,125,040
nssv17690502RemappedPerfectNC_000012.11:g.104
518303_104518818de
l
GRCh37.p13First PassNC_000012.11Chr12104,518,303104,518,818

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)
nssv17690502<0.00116404
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