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nsv5444951

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,205

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 180 SVs from 27 studies. See in: genome view    
Submitted genomic240,818,778-240,820,982Question Mark
Overlapping variant regions from other studies: 183 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):240,982,078-240,984,282Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5444951Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1240,818,778240,820,982
nsv5444951RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1240,982,078240,984,282

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16899453deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16899453Submitted genomicNC_000001.11:g.240
818778_240820982de
l
GRCh38 (hg38)NC_000001.11Chr1240,818,778240,820,982
nssv16899453RemappedPerfectNC_000001.10:g.240
982078_240984282de
l
GRCh37.p13First PassNC_000001.10Chr1240,982,078240,984,282

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)
nssv16899453<0.00116404
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