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nsv5465497

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:93

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 137 SVs from 28 studies. See in: genome view    
Submitted genomic141,219,432-141,219,524Question Mark
Overlapping variant regions from other studies: 137 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):142,140,586-142,140,678Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5465497Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4141,219,432141,219,524
nsv5465497RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4142,140,586142,140,678

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16956341deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16956341Submitted genomicNC_000004.12:g.141
219432_141219524de
l
GRCh38 (hg38)NC_000004.12Chr4141,219,432141,219,524
nssv16956341RemappedPerfectNC_000004.11:g.142
140586_142140678de
l
GRCh37.p13First PassNC_000004.11Chr4142,140,586142,140,678

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)
nssv169563410.003176404
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