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nsv4508603

  • 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: 20 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):50,862,203-50,862,203Question Mark
Overlapping variant regions from other studies: 19 SVs from 5 studies. See in: genome view    
Submitted genomic48,939,564-48,939,564Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4508603RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1750,862,20350,862,203
nsv4508603Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1748,939,56448,939,564

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16017465alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16017465RemappedPerfectNC_000017.11:g.508
62203_50862204ins2
81
GRCh38.p12First PassNC_000017.11Chr1750,862,20350,862,203
nssv16017465Submitted genomicNC_000017.10:g.489
39564_48939565ins2
81
GRCh37.p13NC_000017.10Chr1748,939,56448,939,564

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)
nssv160174650.00715321688
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