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nsv5535972

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:530,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2406 SVs from 100 studies. See in: genome view    
Submitted genomic20,679,564-21,209,564Question Mark
Overlapping variant regions from other studies: 2407 SVs from 100 studies. See in: genome view    
Remapped(Score: Perfect):21,033,852-21,563,853Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5535972Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2220,679,56421,209,564
nsv5535972RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2221,033,85221,563,853

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17727728deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17727728Submitted genomicNC_000022.11:g.206
79564_21209564del
GRCh38 (hg38)NC_000022.11Chr2220,679,56421,209,564
nssv17727728RemappedPerfectNC_000022.10:g.210
33852_21563853del
GRCh37.p13First PassNC_000022.10Chr2221,033,85221,563,853

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)
nssv17727728<0.00116404
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