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nsv5547252

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 142 SVs from 24 studies. See in: genome view    
Submitted genomic227,767,174-227,767,223Question Mark
Overlapping variant regions from other studies: 145 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):227,954,875-227,954,924Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5547252Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1227,767,174227,767,223
nsv5547252RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1227,954,875227,954,924

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16897463insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16897463Submitted genomicNC_000001.11:g.227
767174_227767223in
s149
GRCh38 (hg38)NC_000001.11Chr1227,767,174227,767,223
nssv16897463RemappedPerfectNC_000001.10:g.227
954875_227954924in
s149
GRCh37.p13First PassNC_000001.10Chr1227,954,875227,954,924

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)
nssv16897463<0.00116404
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