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nsv5553466

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 72 SVs from 16 studies. See in: genome view    
Submitted genomic100,451,798-100,451,807Question Mark
Overlapping variant regions from other studies: 72 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):100,170,642-100,170,651Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5553466Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3100,451,798100,451,807
nsv5553466RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3100,170,642100,170,651

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16937094insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16937094Submitted genomicNC_000003.12:g.100
451798_100451807in
s57
GRCh38 (hg38)NC_000003.12Chr3100,451,798100,451,807
nssv16937094RemappedPerfectNC_000003.11:g.100
170642_100170651in
s57
GRCh37.p13First PassNC_000003.11Chr3100,170,642100,170,651

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)
nssv169370940.37724136404
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