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nsv5463198

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,307

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 145 SVs from 39 studies. See in: genome view    
Submitted genomic160,228,676-160,233,982Question Mark
Overlapping variant regions from other studies: 145 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):160,649,708-160,655,014Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5463198Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6160,228,676160,233,982
nsv5463198RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6160,649,708160,655,014

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16990818deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16990818Submitted genomicNC_000006.12:g.160
228676_160233982de
l
GRCh38 (hg38)NC_000006.12Chr6160,228,676160,233,982
nssv16990818RemappedPerfectNC_000006.11:g.160
649708_160655014de
l
GRCh37.p13First PassNC_000006.11Chr6160,649,708160,655,014

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)
nssv169908180.012766404
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