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nsv5467971

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:107

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 126 SVs from 20 studies. See in: genome view    
Submitted genomic89,579,523-89,579,629Question Mark
Overlapping variant regions from other studies: 126 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):90,289,242-90,289,348Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5467971Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr689,579,52389,579,629
nsv5467971RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr690,289,24290,289,348

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16985367deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16985367Submitted genomicNC_000006.12:g.895
79523_89579629del
GRCh38 (hg38)NC_000006.12Chr689,579,52389,579,629
nssv16985367RemappedPerfectNC_000006.11:g.902
89242_90289348del
GRCh37.p13First PassNC_000006.11Chr690,289,24290,289,348

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)
nssv16985367<0.00116404
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