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nsv5437126

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,657

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 157 SVs from 31 studies. See in: genome view    
Submitted genomic126,690,162-126,693,818Question Mark
Overlapping variant regions from other studies: 157 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):127,447,738-127,451,394Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5437126Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2126,690,162126,693,818
nsv5437126RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2127,447,738127,451,394

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16919512deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16919512Submitted genomicNC_000002.12:g.126
690162_126693818de
l
GRCh38 (hg38)NC_000002.12Chr2126,690,162126,693,818
nssv16919512RemappedPerfectNC_000002.11:g.127
447738_127451394de
l
GRCh37.p13First PassNC_000002.11Chr2127,447,738127,451,394

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)
nssv169195120.00176404
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