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nsv5502973

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:563

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 65 SVs from 20 studies. See in: genome view    
Submitted genomic8,098,274-8,098,836Question Mark
Overlapping variant regions from other studies: 65 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):8,119,821-8,120,383Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5502973Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr118,098,2748,098,836
nsv5502973RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr118,119,8218,120,383

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17041835duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17041835Submitted genomicNC_000011.10:g.809
8274_8098836dup
GRCh38 (hg38)NC_000011.10Chr118,098,2748,098,836
nssv17041835RemappedPerfectNC_000011.9:g.8119
821_8120383dup
GRCh37.p13First PassNC_000011.9Chr118,119,8218,120,383

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)
nssv17041835<0.00116404
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