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nsv5495315

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:228,765

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1357 SVs from 79 studies. See in: genome view    
Submitted genomic19,638,004-19,866,768Question Mark
Overlapping variant regions from other studies: 1357 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):20,212,144-20,440,908Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5495315Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1319,638,00419,866,768
nsv5495315RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1320,212,14420,440,908

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17685893duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17685893Submitted genomicNC_000013.11:g.196
38004_19866768dup
GRCh38 (hg38)NC_000013.11Chr1319,638,00419,866,768
nssv17685893RemappedPerfectNC_000013.10:g.202
12144_20440908dup
GRCh37.p13First PassNC_000013.10Chr1320,212,14420,440,908

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)
nssv17685893<0.00116404
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