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nsv5915318

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:194

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 210 SVs from 33 studies. See in: genome view    
Submitted genomic86,927,111-86,927,304Question Mark
Overlapping variant regions from other studies: 210 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):88,686,868-88,687,061Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5915318Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1086,927,11186,927,304
nsv5915318RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1088,686,86888,687,061

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17363058duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17363058Submitted genomicNC_000010.11:g.869
27111_86927304dup
GRCh38 (hg38)NC_000010.11Chr1086,927,11186,927,304
nssv17363058RemappedPerfectNC_000010.10:g.886
86868_88687061dup
GRCh37.p13First PassNC_000010.10Chr1088,686,86888,687,061

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)
nssv173630580.00111660
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