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nsv5464368

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 21 studies. See in: genome view    
Submitted genomic142,173,556-142,173,626Question Mark
Overlapping variant regions from other studies: 91 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):142,494,693-142,494,763Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5464368Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6142,173,556142,173,626
nsv5464368RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6142,494,693142,494,763

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16970307deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16970307Submitted genomicNC_000006.12:g.142
173556_142173626de
l
GRCh38 (hg38)NC_000006.12Chr6142,173,556142,173,626
nssv16970307RemappedPerfectNC_000006.11:g.142
494693_142494763de
l
GRCh37.p13First PassNC_000006.11Chr6142,494,693142,494,763

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)
nssv16970307<0.00116404
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