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nsv5455858

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,442

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 148 SVs from 40 studies. See in: genome view    
Submitted genomic141,387,659-141,398,100Question Mark
Overlapping variant regions from other studies: 146 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):140,767,226-140,777,667Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5455858Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5141,387,659141,398,100
nsv5455858RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5140,767,226140,777,667

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16975415deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16975415Submitted genomicNC_000005.10:g.141
387659_141398100de
l
GRCh38 (hg38)NC_000005.10Chr5141,387,659141,398,100
nssv16975415RemappedPerfectNC_000005.9:g.1407
67226_140777667del
GRCh37.p13First PassNC_000005.9Chr5140,767,226140,777,667

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)
nssv16975415<0.00156394
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