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nsv4564279

  • 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: 29 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):22,217,379-22,217,379Question Mark
Overlapping variant regions from other studies: 29 SVs from 4 studies. See in: genome view    
Submitted genomic22,198,017-22,198,017Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4564279RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2022,217,37922,217,379
nsv4564279Submitted genomicGRCh37.p13Primary AssemblyNC_000020.10Chr2022,198,01722,198,017

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16032310line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16032310RemappedPerfectNC_000020.11:g.222
17379_22217380ins1
239
GRCh38.p12First PassNC_000020.11Chr2022,217,37922,217,379
nssv16032310Submitted genomicNC_000020.10:g.221
98017_22198018ins1
239
GRCh37.p13NC_000020.10Chr2022,198,01722,198,017

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)
nssv160323104.6e-005121694
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