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nsv5949510

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:166

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 26 studies. See in: genome view    
Submitted genomic46,227,988-46,228,153Question Mark
Overlapping variant regions from other studies: 121 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):44,856,627-44,856,792Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5949510Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2046,227,98846,228,153
nsv5949510RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2044,856,62744,856,792

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17399962duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17399962Submitted genomicNC_000020.11:g.462
27988_46228153dup
GRCh38 (hg38)NC_000020.11Chr2046,227,98846,228,153
nssv17399962RemappedPerfectNC_000020.10:g.448
56627_44856792dup
GRCh37.p13First PassNC_000020.10Chr2044,856,62744,856,792

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)
nssv173999620.00341538
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