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nsv5460508

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:508

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 680 SVs from 63 studies. See in: genome view    
Submitted genomic467,447-467,954Question Mark
Overlapping variant regions from other studies: 680 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):467,562-468,069Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5460508Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5467,447467,954
nsv5460508RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5467,562468,069

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17743020deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17743020Submitted genomicNC_000005.10:g.467
447_467954del
GRCh38 (hg38)NC_000005.10Chr5467,447467,954
nssv17743020RemappedPerfectNC_000005.9:g.4675
62_468069del
GRCh37.p13First PassNC_000005.9Chr5467,562468,069

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)
nssv177430200.30519536404
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