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nsv5917369

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 41 studies. See in: genome view    
Submitted genomic114,601,515-114,601,585Question Mark
Overlapping variant regions from other studies: 162 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):114,472,237-114,472,307Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5917369Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11114,601,515114,601,585
nsv5917369RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11114,472,237114,472,307

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17360541duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17360541Submitted genomicNC_000011.10:g.114
601515_114601585du
p
GRCh38 (hg38)NC_000011.10Chr11114,601,515114,601,585
nssv17360541RemappedPerfectNC_000011.9:g.1144
72237_114472307dup
GRCh37.p13First PassNC_000011.9Chr11114,472,237114,472,307

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)
nssv1736054112222
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