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nsv5473790

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 144 SVs from 24 studies. See in: genome view    
Submitted genomic181,204,612-181,204,663Question Mark
Overlapping variant regions from other studies: 144 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):180,631,612-180,631,663Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5473790Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5181,204,612181,204,663
nsv5473790RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5180,631,612180,631,663

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16977882deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16977882Submitted genomicNC_000005.10:g.181
204612_181204663de
l
GRCh38 (hg38)NC_000005.10Chr5181,204,612181,204,663
nssv16977882RemappedPerfectNC_000005.9:g.1806
31612_180631663del
GRCh37.p13First PassNC_000005.9Chr5180,631,612180,631,663

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)
nssv169778820.002126404
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