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nsv5534645

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 112 SVs from 19 studies. See in: genome view    
Submitted genomic207,065,224-207,065,226Question Mark
Overlapping variant regions from other studies: 116 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):207,238,569-207,238,571Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5534645Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1207,065,224207,065,226
nsv5534645RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1207,238,569207,238,571

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16894969insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16894969Submitted genomicNC_000001.11:g.207
065224_207065226in
s522
GRCh38 (hg38)NC_000001.11Chr1207,065,224207,065,226
nssv16894969RemappedPerfectNC_000001.10:g.207
238569_207238571in
s522
GRCh37.p13First PassNC_000001.10Chr1207,238,569207,238,571

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)
nssv16894969<0.00116404
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