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nsv4573458

  • 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: 39 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):31,886,517-31,886,517Question Mark
Overlapping variant regions from other studies: 39 SVs from 7 studies. See in: genome view    
Submitted genomic30,474,320-30,474,320Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573458RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2031,886,51731,886,517
nsv4573458Submitted genomicGRCh37.p13Primary AssemblyNC_000020.10Chr2030,474,32030,474,320

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16033003line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16033003RemappedPerfectNC_000020.11:g.318
86517_31886518ins6
019
GRCh38.p12First PassNC_000020.11Chr2031,886,51731,886,517
nssv16033003Submitted genomicNC_000020.10:g.304
74320_30474321ins6
019
GRCh37.p13NC_000020.10Chr2030,474,32030,474,320

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)
nssv160330030.0049621676
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