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nsv5522221

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:989

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 158 SVs from 27 studies. See in: genome view    
Submitted genomic74,921,169-74,922,157Question Mark
Overlapping variant regions from other studies: 158 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):75,213,510-75,214,498Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5522221Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1574,921,16974,922,157
nsv5522221RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1575,213,51075,214,498

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702037duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702037Submitted genomicNC_000015.10:g.749
21169_74922157dup
GRCh38 (hg38)NC_000015.10Chr1574,921,16974,922,157
nssv17702037RemappedPerfectNC_000015.9:g.7521
3510_75214498dup
GRCh37.p13First PassNC_000015.9Chr1575,213,51075,214,498

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)
nssv17702037<0.00126404
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