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nsv4502154

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 15 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):47,295,413-47,295,413Question Mark
Overlapping variant regions from other studies: 13 SVs from 4 studies. See in: genome view    
Submitted genomic45,372,779-45,372,779Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4502154RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1747,295,41347,295,413
nsv4502154Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1745,372,77945,372,779

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16015200alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16015200RemappedPerfectNC_000017.11:g.472
95413_47295414ins2
05
GRCh38.p12First PassNC_000017.11Chr1747,295,41347,295,413
nssv16015200Submitted genomicNC_000017.10:g.453
72779_45372780ins2
05
GRCh37.p13NC_000017.10Chr1745,372,77945,372,779

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)
nssv160152004.6e-005121694
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