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nsv5467245

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,877

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 139 SVs from 33 studies. See in: genome view    
Submitted genomic73,203,525-73,205,401Question Mark
Overlapping variant regions from other studies: 139 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):74,069,242-74,071,118Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5467245Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr473,203,52573,205,401
nsv5467245RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr474,069,24274,071,118

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16952231deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16952231Submitted genomicNC_000004.12:g.732
03525_73205401del
GRCh38 (hg38)NC_000004.12Chr473,203,52573,205,401
nssv16952231RemappedPerfectNC_000004.11:g.740
69242_74071118del
GRCh37.p13First PassNC_000004.11Chr474,069,24274,071,118

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)
nssv16952231<0.00116404
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