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nsv5453324

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,052

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 21 studies. See in: genome view    
Submitted genomic211,807,271-211,808,322Question Mark
Overlapping variant regions from other studies: 125 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):211,980,613-211,981,664Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5453324Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1211,807,271211,808,322
nsv5453324RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1211,980,613211,981,664

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16895084deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16895084Submitted genomicNC_000001.11:g.211
807271_211808322de
l
GRCh38 (hg38)NC_000001.11Chr1211,807,271211,808,322
nssv16895084RemappedPerfectNC_000001.10:g.211
980613_211981664de
l
GRCh37.p13First PassNC_000001.10Chr1211,980,613211,981,664

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)
nssv16895084<0.00156404
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