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nsv5545014

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:34

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 279 SVs from 31 studies. See in: genome view    
Submitted genomic45,914,223-45,914,256Question Mark
Overlapping variant regions from other studies: 277 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):43,991,589-43,991,622Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5545014Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1745,914,22345,914,256
nsv5545014RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1743,991,58943,991,622

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713399insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713399Submitted genomicNC_000017.11:g.459
14223_45914256ins6
0
GRCh38 (hg38)NC_000017.11Chr1745,914,22345,914,256
nssv17713399RemappedPerfectNC_000017.10:g.439
91589_43991622ins6
0
GRCh37.p13First PassNC_000017.10Chr1743,991,58943,991,622

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)
nssv177133990.0945696074
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