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nsv5473625

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:189,712

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 474 SVs from 52 studies. See in: genome view    
Submitted genomic49,690,434-49,880,145Question Mark
Overlapping variant regions from other studies: 474 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):49,658,147-49,847,858Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5473625Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr649,690,43449,880,145
nsv5473625RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr649,658,14749,847,858

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16983261deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16983261Submitted genomicNC_000006.12:g.496
90434_49880145del
GRCh38 (hg38)NC_000006.12Chr649,690,43449,880,145
nssv16983261RemappedPerfectNC_000006.11:g.496
58147_49847858del
GRCh37.p13First PassNC_000006.11Chr649,658,14749,847,858

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)
nssv16983261<0.00116404
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