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nsv5521125

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,758

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 93 SVs from 29 studies. See in: genome view    
Submitted genomic11,619,627-11,626,384Question Mark
Overlapping variant regions from other studies: 93 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):11,713,483-11,720,240Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5521125Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1611,619,62711,626,384
nsv5521125RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1611,713,48311,720,240

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17704588deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17704588Submitted genomicNC_000016.10:g.116
19627_11626384del
GRCh38 (hg38)NC_000016.10Chr1611,619,62711,626,384
nssv17704588RemappedPerfectNC_000016.9:g.1171
3483_11720240del
GRCh37.p13First PassNC_000016.9Chr1611,713,48311,720,240

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)
nssv17704588<0.00116404
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