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nsv5548736

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:190,327

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2128 SVs from 105 studies. See in: genome view    
Submitted genomic22,174,185-22,364,511Question Mark
Overlapping variant regions from other studies: 2140 SVs from 105 studies. See in: genome view    
Remapped(Score: Good):22,528,571-22,718,871Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5548736Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2222,174,18522,364,511
nsv5548736RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2222,528,57122,718,871

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17727853duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17727853Submitted genomicNC_000022.11:g.221
74185_22364511dup
GRCh38 (hg38)NC_000022.11Chr2222,174,18522,364,511
nssv17727853RemappedGoodNC_000022.10:g.225
28571_22718871dup
GRCh37.p13First PassNC_000022.10Chr2222,528,57122,718,871

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)
nssv17727853<0.00116314
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