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nsv5400716

  • 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: 75 SVs from 20 studies. See in: genome view    
Submitted genomic164,509,449-164,509,500Question Mark
Overlapping variant regions from other studies: 75 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):163,936,455-163,936,506Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5400716Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5164,509,449164,509,500
nsv5400716RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5163,936,455163,936,506

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16976525alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16976525Submitted genomicNC_000005.10:g.164
509449_164509500in
s281
GRCh38 (hg38)NC_000005.10Chr5164,509,449164,509,500
nssv16976525RemappedPerfectNC_000005.9:g.1639
36455_163936506ins
281
GRCh37.p13First PassNC_000005.9Chr5163,936,455163,936,506

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)
nssv16976525<0.00156404
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